Category Archives: Cell Biology

North America $81 Billion Life Science Tools Market to 2027: Growth of Cell & Gene Therapies & Increasing Demand for Biopharmaceuticals -…

DUBLIN, March 10, 2021 /PRNewswire/ -- The "North America Life Science Tools Market Size, Share & Trends Analysis Report by End-use, by Technology (Cell Biology, Proteomics Technologies), by Product (PCR & qPCR, Cell Biology), and Segment Forecasts, 2020-2027" report has been added to ResearchAndMarkets.com's offering.

The North America life science tools market size is expected to reach USD 81.9 billion by 2027 registering a CAGR of 11.6%

The market growth is attributed to a rise in government funding for life science technologies, growth of cell & gene therapies, increasing demand for biopharmaceuticals, and a rise in competition among prominent market entities.

Competitive dynamics continue to drive a rapid pace of innovation in sequencing, multiplex platforms, and major categories of mass spectrometry and liquid chromatography; this supports growth via upgrade/replacement cycles and expands the applicability of technologies. An increase in investments for R&D of life science tools is expected to drive the market significantly.

For instance, Thermofisher Scientific, one of the leading players in the market, increased its R&D expenditure by 7.32% to USD 0.264 billion year-over-year by the quarter ending June 30, 2020. A rise in the number of strategic deals & developments coupled with the steady commercial success of biopharmaceuticals is expected to accelerate market growth over the forecast period.

The Bristol-Myers Squibb/Celgene acquisition (USD 74 billion), AbbVie/Allergan acquisition (USD 63 billion), Takeda/Shire acquisition (USD 58.6 billion), Danaher and GE Biopharma M&A deal (USD 21.4 billion), Amgen / Celgene's Otezla deal (USD 13.4 billion), and Pfizer/Array Biopharma merger (USD 11.4 billion) were some of the largest biopharma merger and acquisition deals of 2019.

Key Topics Covered:

Chapter 1 Methodology and Scope1.1 Research Assumptions1.2 Research Methodology1.3 Information Procurement1.4 Information or Data Analysis1.5 Market Formulation & Validation1.6 Market Model1.6.1 Nucleic Acid Preparation market1.6.2 Cell biology market1.6.2.1 Comparison of 3D cell culture techniques1.6.3 Next-Generation Sequencing & Transfection Electroporation market1.6.4 Market study, by Technology1.6.5 QFD modeling for market share assessment of technologies1.6.6 Market study, by end use1.7 Global Market: CAGR Calculation1.8 Objectives

Chapter 2 Executive Summary2.1 Market Summary, 2019

Chapter 3 Market Variables, Trends, & Scope3.1 Market Dynamics3.1.1 Market driver analysis3.1.1.1 Increased government funding for life science technologies3.1.1.2 Growth of cell and gene therapies3.1.1.3 Rise in demand for biopharmaceuticals (biologics and biosimilars)3.1.1.4 Technological advancements in life science tools3.1.1.5 Applications of genomic and proteomic technologies for precision medicine3.1.2 Market restraint analysis3.1.2.1 High cost for some technologies3.1.2.2 Dearth of skilled professionals3.1.3 Market opportunity analysis3.1.3.1 Rise in the number of strategic deals & developments3.2 Penetration and Growth Prospect Mapping for Technology, 2019 (USD Million)3.3 Impact of COVID-19 pandemic on North America Life Science Tools Market3.3.1 Impact on the supply chain3.3.2 Impact on life sciences & healthcare industry3.4 Market Share Analysis3.4.1 Company Size3.4.2 Product portfolio3.4.3 Strategic Initiatives3.5 Business Environment Analysis3.5.1 SWOT Analysis; By factor (Political & Legal, Economic, and Technological)3.5.2 Porter's Five Forces Analysis

Chapter 4 Technology Movement Analysis4.1 Market: Technology Movement Analysis4.2 Genomic Technology4.3 Proteomics Technology4.4 Cell Biology Technology4.5 Other Analytical & Sample Preparation Technology4.6 Lab Supplies & Technologies

Chapter 5 Product Business Analysis5.1 North America Life Science Tools Market: Product Movement Analysis5.2 Next-Generation Sequencing5.2.1 Market estimates and forecast for NGS, 2016-2027 (USD Million)5.2.2 Instruments5.2.3 Consumables5.2.4 Services5.3 PCR & qPCR5.4 Flow Cytometry5.5 Nuclear Magnetic Resonance Spectroscopy (NMR)5.6 Microscopy & Electron Microscopy5.7 Liquid Chromatography (LC)5.8 Mass Spectrometry (MS)5.9 Nucleic Acid Preparation (NAP)5.10 Transfection Electroporation5.11 Cell Biology5.12 Cloning5.13 Other products & services5.13.1 Market for other products & services, 2016-2027 (USD Million)5.13.2 Antibodies5.13.3 General supplies5.13.4 Nucleic Acid Microarray5.13.4.1 Instruments5.13.4.2 Consumables5.13.4.3 Services5.13.5 Others5.13.5.1 Market for others, 2016-2027 (USD Million)5.13.5.2 Instruments5.13.5.3 Consumables5.13.5.4 Services

Chapter 6 End-use Movement Analysis6.1 Market: End-use Movement Analysis6.2 Government & Academic6.3 Biopharmaceutical Company6.4 Healthcare6.5 Industrial Application

Chapter 7 Regional Movement Analysis

Chapter 8 Company Profiles

For more information about this report visit https://www.researchandmarkets.com/r/wp7omn

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North America $81 Billion Life Science Tools Market to 2027: Growth of Cell & Gene Therapies & Increasing Demand for Biopharmaceuticals -...

Explore the Cell Expansion Market: Ethical Concerns Regarding Research in Cell Biology – WhaTech

The Global Cell Expansion Market size is estimated to be USD 14.9 billion in 2020 and projected to reach USD 30.1 billion by 2025, at a CAGR of 15.1%. Cell Expansion Market by Product (Reagent, Media, Flow Cytometer, Centrifuge, Bioreactor), Cell Type (Human, Animal), Application (Regenerative Medicine & Stem Cell Research, Cancer & Cell-based Research), End-User, and Region - Global Forecast to 2025

The Cell Expansion Market size is estimated to be USD 14.9 billion in 2020 and projected to reach USD 30.1 billion by 2025, at a CAGR of 15.1%.

Growth in this market is primarily driven by the increasing incidence of chronic diseases, government investments for cell-based research, growing focus on personalized medicine, increasing focus on R&D for cell-based therapies, and increasing GMP certifications for cell therapy production facilities.

The media segment accounted for the largest share of the consumables segment in the cell expansion market

Based on product type, consumables are segmented into media, reagents, sera, and disposables. The media segment accounted for the largest share of the consumables segment in the cell expansion market.

The large share of this segment can be attributed to its high requirement during the production of pharmaceutical products and rising R&D investments on cell-based therapies.

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Biotechnology & biopharmaceutical companies accounted for the fastest-growing end user segment of the cell expansion market

Based on end-users, the cell expansion industry market has been segmented into research institutes, biotechnology & biopharmaceutical companies, cell banks, and other end users (includes hospitals, diagnostic centers, and laboratories). In 2019, biotechnology & biopharmaceutical companies were the largest end-users in the cell expansion market, and the trend is the same throughout the forecast period.

North America accounted for the largest share of the cell expansion market

North America accounted for the largest share of the cell expansion industry market.

The large share of this segment can primarily be attributed to the rising incidence of cancer, increasing government funding, rising research activates on stem cell therapies, growing awareness regarding advanced treatment methods, increasing geriatric population, and the strong presence of industry players in the region.

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Leading Companies

Thermo Fisher Scientific, Inc. (US), Danaher (US), Becton, Dickinson and Company (US), Lonza (Switzerland), Corning, Inc. (US), Merck KGaA (Germany), Sartorius Stedim Biotech (France), Getinge AB (Sweden) Terumo Corporation (Japan), and Miltenyi Biotec (Germany)

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Peer Recognition | The UCSB Current – The UCSB Current

Three professors from the UC Santa Barbara College of Engineering and one from the Department of Molecular, Cellular and Developmental Biology (MCDB) have been named Fellows of the prestigious American Institute for Medical and Biological Engineering (AIMBE), recognizing their interdisciplinary achievements.

Nominated by their peers, fellows represent the top 2% of the medical and biological engineering community.

Mechanical engineers Linda Petzold, Sumita Pennathur and Megan Valentine, and MCDBs Dennis Clegg, are among this years 174 new AIMBE fellows. Members are nominated by their peers and represent the top two percent of the medical and biological engineering community, having made transformational contributions to the medical and biological engineering (MBE) community in academia, industry, government and education.

We are extremely proud to have four UC Santa Barbara faculty members selected as AIMBE Fellows for 2021, saidRod Alferness, dean of the UCSB College of Engineering. Being named an AIMBE Fellow is a particularly notable achievement, first, because it is highly competitive and second, and perhaps more importantly, because it recognizes achievements at the intersection of science and engineering, which may have life-changing impacts. We offer our most sincere congratulations to Linda Petzold, Sumita Pennathur, Megan Valentine and Dennis Clegg on this significant achievement.

I congratulate all four professors from UC Santa Barbara on this honor, said Pierre Wiltzius, the Susan & Bruce Worster Dean of Science in the College of Letters & Science. AIMBE Fellows are known foremost for their transformative interdisciplinary research, which is something we champion on this campus. Our faculty have a long and fruitful history of integrating science and engineering, and I couldnt be happier to see the work of these leading scholars recognized.

Linda Petzold, also a professor of computer science, has been widely recognized for her impactful work on mathematical modeling and computational simulation in a variety of disciplines and applications. Her breakthrough 1982 paper Differential-Algebraic Equations (DAEs) are not ODEs [ordinary differential equations] opened up a new subfield in computational mathematics, and her public-domain software DASSL has enabled the simulation of countless systems in engineering and science.

It is a pleasure for me to receive this recognition from the AIMBE community for my work in medical and biological engineering, she said.I greatly enjoy working in this area, as it allows me the opportunity to address challenges and further understanding in a variety of diverse subject areas.

Petzolds algorithm and software (LSODA), described in a 1983 paper, has been used extensively and remains in widespread use, in particular as part of Mathematica (a modern and widely applied technical computing system), as well as in the chemical and pharmaceutical industries. More recently, her work has focused on algorithms and software for discrete stochastic systems, motivated by the need to model the inherent randomness of biochemical reactions in the cell. In this work, she and her collaborators have developed algorithms and the public-domain software StochSS for discrete stochastic simulation of biochemical systems. Her work on mathematical modeling of biological systems has elucidated a mechanism for the onset of coagulopathy, revealed the role of stochasticity in cell polarization, derived the network structure of neurons involved in Circadian Rhythm, and contributed in numerous other areas.

Petzold, a member of the National Academy of Engineering, has contributed extensively to the profession and to diversity in the sciences. She serves on the Board of Directors of the Society for Industrial and Applied Mathematics (SIAM), in 2016 receiving the SIAM Prize for Distinguished Service to the Profession. Committed to promoting and supporting diversity in the profession, she has served as director of the UCSB Institute for Collaborative Biotechnologies Diversity Program, focused on underrepresented students with a special emphasis on women in science.

Sumita Pennathur, a pioneer in nanofluidics, interfacial science and biological engineering,has a longstanding commitment to advancing human health through innovative science and engineering. Her seminal work has revealed unique physics at the nanoscale, making it possible to model, predict and, ultimately, control fluids and the molecules they contain. Researchers in the Pennathur laboratory invent, design and build nanoscale devices to measure key fluidic parameters with unprecedented accuracy and precision via a tight integration of theory, modeling and reduction to practice.

Pennathur has applied her discoveries to develop novel biomedical technologies, leading her to found three startup companies:Asta Fluidics, for rapid diagnosis of potentially lethal complications during pregnancy;Alveo Technologies, which is developing an in-home diagnostic for COVID-19; and Laxmi Therapeutic Devices,amicroneedle based continuous glucose monitoring company.

I am honored to be recognized alongside a cohort of amazing biomedical engineers and innovators, Pennathur said. I fully supportthe AIMBE mission to advance medicine and bioengineering innovations and commend the society of their impact in funding for medical science and education.

For her early academic research accomplishments, Pennathur in 2010 received a coveted PECASE award (Presidential Early Career Awards for Scientists and Engineers) from President Obama. She also was awarded the Defense Advanced Research Programs Administration (DARPA) Young Faculty Award in 2008, the UC Regents Junior Faculty Fellowship in 2009, and the ADA Pathway to Stop Diabetes Visionary Award in 2017.

Megan Valentine is an internationally recognized leader in biomaterials science, cellular mechanics and mechanotransduction. Her pioneering research establishes how forces are generated, transmitted and sensed in soft living matter, and how to capture the properties of living systems in synthetic materials. Her innovative approaches bridge length scales from molecular to macroscopic and combine her significant biological expertise with innovative tool development and a deep understanding of physical phenomena to impact multiple areas of biomedical engineering.

It's an honor to be selected as an AIMBE Fellow and a testament to the collaborative and interdisciplinary nature of both my work and UC Santa Barbara, Valentine said. Ive dedicated my career to working across disciplines: my undergraduate and graduate degrees are in physics, I completed a post-doc in biological sciences and am a professor of mechanical engineering. Each specialty has its own jargon and culture, and I am proud that my ability to innovate across boundaries has been recognized. I am eager to continue working with doctors, scientists and engineers from diverse communities to address pressing societal needs.

Valentines groundbreaking studies have provided a critically important understanding of the molecular mechanisms underlying normal cell division. Her work has established the use of microrheology for unprecedented measurements of the interplay among structure, mechanics and dynamics of complex biomaterials, such as cytoplasm.

By developing innovative imaging methods and mechanical testing devices, she has established the role of mechanosensation in regulating vascular growth dynamics, as well as the response of cells to high strain and high strain-rate impacts, providing novel insight into vascular regeneration and traumatic brain injury, respectively.

Finally, Valentine has become a leader in the area of bio-inspired materials, with an emphasis on developing high-performance adhesives and load-bearing composites. She established the nonlinear elastic and fracture behavior of natural materials, and is developing new classes of strong stimuli-responsive polymeric materials, with applications to healthcare, packaging and robotics.

Valentine is a devoted advocate for women and underrepresented minority students both at UCSB and in the broader bioengineering community. Particularly invested in engaging student veterans in hands-on research, she has developed two NSF-supported programs to support their summer internships at UCSB.

She is an active organizer in the American Physical Society March Meeting, and recently completed a three-year term on the Executive Committee of the Division of Biological Physics. She has served as a member of the Early Careers Committee of the Biophysical Society, where she led efforts in advocacy, training and professional development for graduate students and postdoctoral scholars. An AIMBE fellowship will provide her with new avenues of engagement and new opportunities to work for the betterment of our community and society.

Valentine is a co-director of the California NanoSystems Institute (CNSI) at UCSB and a fellow of the American Physical Society. She received a Career Award at the Scientific Interface (CASI) from the Burroughs Wellcome Fund, a UC Regents Junior Faculty Fellowship, a Hellman Family Faculty Fund Fellowship, a CAREER award from the National Science Foundation, and a Fulbright Scholar Award from the U.S. Department of State.

Dennis Clegg, a pioneer in translational regenerative medicine, achieved world renown for developing a bioengineered implant consisting of stem-cell-derived retinal cells on a synthetic parylene membrane. The technology is now in clinical trials for the treatment of dry age-related macular degeneration (AMD), a leading cause of blindness.

Cleggs lab discovered methods to differentiate pluripotent stem cells into retinal pigmented epithelial (RPE) cells, which degenerate in AMD. His group was the first to report that bona fide RPE cells could be derived from induced pluripotent stem cells (iPS). He established and is co-PI of the California Project to Cure Blindness, a multidisciplinary team comprising stem cell biologists, engineers and surgeons who developed the RPE implant and devised a surgical delivery strategy. Their Phase I trial has generated promising results for the dry form of AMD, a blinding condition with no treatment.

This is a great honor; it underscores the importance of thinking outside the disciplinary box, and collaboration between biologists and engineers, Clegg said of this election as an AIMBE Fellow. UCSB has provided a fertile ground for cutting-edge work, which will continue to thrive, resulting in advances in biomedical engineering.

Clegg has made impactful contributions to our understanding of cell-extracellular matrix interactions during ocular development. These studies informed further research of novel bio-mimetic materials that support survival and differentiation of stem cells. Clegg has navigated these discoveries all the way to clinical application.

Chair of MCDB from 2004-2009, and founder and co-director, since 2008, of the Center for Stem Cell Biology and Engineering, Clegg has served on the Chancellors Committee on Diversity, as director of an HHMI Undergraduate Program, and as director of two graduate training programs aimed at promoting underrepresented minorities and women in science. He was a speaker at the California Graduate Diversity Forum (2006-2014) and currently serves on Scientific Advisory Boards for biotechnology programs at California State University Channel Islands, which, like UCSB, is a Hispanic-Serving Institution.

Clegg also is noted for his ability to communicate complex science to general audiences, as evidenced in his 2012 TedX talk and in his extensive public outreach, particularly in educational activities related to stem cell biology and regenerative medicine.

All 160 members of the AIMBE College of Fellows Class of 2021 will be inducted at a ceremony to be held remotely March 26.

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Super-resolution system microscopy can reveal pluripotency and differentiation of live stem cells – News-Medical.net

A new super-resolution system microscopy can assess the pluripotency and differentiation of live stem cells, spearheading a new era in stem-cell research and systems biology. This technology can help in cancer research and development of treatments

You might have heard about "stem cells" in the news or in popular science documentaries and wondered if they could one day help you or a loved one treat an injury or a serious disease. Indeed, since their initial discovery in the 1960s there has been a growing interest in research and treatments in this field.

For the uninitiated, stems cells are essentially the body's raw materials. Found in embryos as well as in adults, they are cells from which all other cells with specialised functions are generated. Under the right conditions, in the body or in a laboratory, stem cells divide to form "daughter cells".

These daughters can either become new stem cells (self-renewal) or become specialised cells (differentiation) with a more specific function, such as blood cells, brain cells, heart muscle cells or bone cells.

No other cells in the body has the natural ability to generate new cell types. To better understand and exploit their potential, an FET open project called CellViewer was launched in 2016. Led by the Fundacio Institut De Ciencies Fotoniques in Barcelona, it brought together internationally recognized academic and industry experts in the fields of stem cell and chromatin biology, super-resolution microscopy, quantitative modeling of biological systems, and hardware and software development. The aim was to develop a prototype of a high-throughput super-resolution automated microscope that can visualize single live cells at the DNA, mRNA and proteins levels.

In a first application of the technology, CellViewer studied the self-renewal and differentiation of mouse embryonic stem cells (mESC) during specific stimuli. Single, live cells were cultured in pluripotency or differentiation conditions to obtain high resolution images of the stem cell genes, mRNA and proteins of interest. Software programs developed by the project were then used to collect all the high-resolution data and develop predictive models revealing the pluripotency or differentiation state of the cells.

Combined with automation software, the super resolution microscope doesn't require users to have in-depth knowledge about the machine, making it both more broadly accessible and affordable. Indeed, one of the main achievements of CellViewer is the HERMES SR project, funded under the FET Innovation Launchpad, which built a super resolution microscope capable of very fast imaging of many individual cells at the same time. This tool can help detecting and studying cancer samples.

Researchers and doctors hope stem cell studies will help to increase understanding of how diseases occur and to generate healthy cells to replace the diseased ones (regenerative medicine). This research will also aid in testing new drugs for safety and effectiveness, by monitoring how specifically programmed daughter cells react to certain treatments.

The outcomes of the CellViewer project are uniquely suited to bringing systems biology, the computational and mathematical analysis and modelling of complex biological systems, into the era of single cell analysis, which will be a paradigm shift in the way cellular systems can be studied.

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How llamas named Wally and Winter are helping scientists study COVID-19 – UChicago News

McLellan has years of experience working with camelid nanobodies. He and his graduate student Daniel Wrapp, along with Xavier Saelens group in Belgium, have isolated nanobodies that have proven effective against respiratory syncytial virus and two coronaviruses: severe acute respiratory syndrome (SARS) and Middle East respiratory syndrome (MERS).

When the genetic sequence of SARS-CoV-2 was released in January of 2020, McLellan, Wrappand Saelens worked quickly to test whether any of the antibodies that they had previously isolated against the original SARS-CoV (taken from a Belgian llama named Winter) could also bind and neutralize the virus. They discovered that one of these nanobodies, which they had characterized using the Structural Biology Center beamlines at the Advanced Photon Source,might be effective against SARS-CoV-2. McLellan said this nanobodycalled VHH72is now under development as a treatment for COVID-19. He and Wrapp received a2020 Golden Goose Awardfor this research.

McLellan will tell you that while his results were good, his hopes were a little higher.

We were seeking one potent antibody that neutralized all coronaviruses, he said. We immunized Winter hoping to elicit that one nanobody. And maybe we elicited it, but we didnt isolate it.

Isolating these tiny nanobodies is tricky, since the body generates an enormous number of them and only a small fraction is intended to fight a particular virus. Thats exactly the problem that Yi Shi, professor of cell biology at the University of Pittsburgh, is trying to fix.

In apaper published in Science, Shi and his colleagues unveiled a new advanced mass spectroscopy method of extracting those nanobodies from samples of llama blood. According to Shi and research assistant Yufei Xiang,the papers lead author, the resultis a large set of nanobodies that bind well to the SARS-CoV-2 virus.

This is thousands of times better than the current technology, specifically in its selecting properties, Shi said. We want nanobodies that bind tightly to SARS-CoV-2, and with this method we can get a drug-quality nanobody that is up to 10,000 times more potent.

As with McLellans research, Shis experiment began with a llama, this one named Wally because he resembles (and therefore shares a name with) his black Labrador. The team immunized Wally against SARS-CoV-2, waiting two months for nanobodies to be generated, and then Xiang used their new method to analyze the nanobodies, identify and quantify them. They ended up with 10 million nanobody sequences.

These nanobodies can sit at room temperature for six weeks, and are small enough that they can be aerosolized, meaning they can be inhaled directly to the lungs instead of moving through the bloodstream.

To confirm the nanobodies effectiveness, Cheng Zhang, assistant professor at the University of Pittsburgh, determined structures of the nanobodies bound to the SARS-CoV-2 virus at the National Institute of General Medical Sciences and National Cancer InstituteStructural Biology Facility at theAdvanced Photon Source.

With this method we can discover thousands of distinct, ultrahigh-affinity nanobodies for specific antigen binding, Shi said. These nanobodies may or may not provide a treatment for COVID-19, but the technology used to isolate them will be important in the future.

Most recently, a team of scientists led by the University of Bonn in Germanyreported newly discovered nanobodiesthat bind to SARS-CoV-2 and may prevent what is called mutational escape. Thats the ability of a virus to avoid immune responses by mutating, and a treatment that prevents the virus from doing so would guard against re-infection.

This research team combined several nanobodies into molecules that attack different parts of the virus simultaneously, helping to prevent virus mutations from reducing therapeutic effectiveness. These nanobodies were taken from a llama and an alpaca immunized against the SARS-CoV-2 virus, and out of several million candidates they ended up with four molecules that proved to be effective.

Ian Wilson, professor of structural biology at the Scripps Research Institute in California, led the team that conducted X-ray diffraction studies at GM/CA at the Advanced Photon Source to determine structures of these molecules bound to the virus. (Researchers at the APS do not work with the live virus, but with crystals grown from simulated proteins.)

From crystal structures determined from data collected at APS and the Stanford Synchrotron Radiation Lightsource, we were able to identify the binding sites of the nanobodies on the SARS-CoV-2 receptor binding domain, Wilson said. The X-ray structural information, combined with cryo-electron microscopy data, was used to help design even more potent multivalent antibodies to prevent COVID-19 infection. The X-ray structural work was greatly facilitated by immediate access to the Advanced Photon Source.

Only time (and further tests) will tell whether the various nanobodies will translate into effective treatments against COVID-19. But if they do, well have the lovable llama to thank for it.

The Advanced Photon Source is a U.S. Department of Energy Office of Science User Facility operated by Argonne National Laboratory. Additional funding for beamlines used forCOVID-19research at theAPSis provided by the National Institutes of Health (NIH) and byDOEOffice of Science Biological and Environmental Research. TheAPSoperated for10percent more hours in 2020 than usual to supportCOVID-19research, with the additional time supported by theDOEOffice of Science through the National Virtual Biotechnology Laboratory, a consortium ofDOEnational laboratories focused on response toCOVID-19with funding provided by the CoronavirusCARESAct.

Adapted from an article first published by Argonne National Laboratory.

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Adlai Nortye Announces Formation of its New Scientific Advisory Board – BioSpace

World-leading Experts to Provide Guidance to Advance the Company's Drug Development

HANGZHOU, China, March 7, 2021 /PRNewswire/ -- Adlai Nortye, a global clinical-stage biopharmaceutical company, today announced the formation of its new Scientific Advisory Board (SAB) comprised of five internationally renowned experts. The SAB includes Ronald M. Evans, PhD (Member of the US National Academy of Sciences, Professor at the Salk Institute and Director of the Salk's Gene Expression Laboratory), Tony Hunter, PhD (Member of the US National Academy of Sciences, Professor of Molecular and Cell Biology at the Salk Institute), Jason Pontin (Investor and former senior partner at Flagship Pioneering), Andrew Zhu, MD, PhD (Professor of Medicine at Harvard Medical School) and Wenle Xia, MD (former faculty member at Duke University).

Chaired by Dr. Ronald M. Evans, the inaugural members are leading experts in the areas of oncology, clinical science and life science investment. The SAB will guide and advise the Company as it advances its preclinical and clinical immuno-oncology programs to address unmet medical needs.

"We are excited and honored to have a prestigious and accomplished experts joining as inaugural members of our new Scientific Advisory Board," said Carsten Lu, President and Chief Executive Officer of Adlai Nortye. "Their expertise and insightful perspectives will provide excellent support for the advancement of Adlai Nortye's scientific programs to help patients live longer and live better."

Bios of the SAB members are listed below.

Ronald M. Evans, PhD, SAB Chair

Dr. Ronald M. Evans is a Member of the US National Academy of Sciences, Professor at the Salk Institute, Director of the Salk's Gene Expression Laboratory, and March of Dimes Chair in Molecular and Developmental Biology. Dr. Evans is known for his original discoveries of nuclear hormone receptors (NR). In the 1980s, Dr. Evans successfully cloned the first nuclear hormone receptor, the human glucocorticoid receptor. He then discovered a superfamily of 48 nuclear hormone receptors that uncovered a wealth of previously unrecognized physiologic pathways. Drugs developed to these newly discovered receptors help control sugar, salt, calcium, cholesterol, and fat metabolism. In addition, these discoveries have helped to build a new generation of drugs to battle breast, prostate, colon and pancreatic cancers and leukemia.

Tony Hunter, PhD

Dr. Tony Hunter is a Member of the US National Academy of Sciences, Professor of Molecular and Cell Biology at the Salk Institute and the Renato Dulbecco Chair in Cancer Biology. Dr. Hunter is one of the foremost recognized leaders in the field of cell growth control, growth factor receptors and their signal transduction pathways. He is well known for discovering that tyrosine phosphorylation is a fundamental mechanism for transmembrane-signal and dysregulation of such tyrosine phosphorylation, by activated oncogenic protein tyrosine kinases, is a pivotal mechanism utilized in the malignant transformation of cells. Dr. Hunter's discovery of tyrosine phosphorylation uncovered an entirely new mechanism of signal transduction in physiology and malignancy and led to development of a new class of cancer drugs.

Jason Pontin, Investor

Jason Pontin is a venture capitalist, angel investor, science and technology writer, and former senior partner at Flagship Pioneering. He is a Venture Partner at Social Impact Capital, Partner at TK, the board chair and cofounder of Totus Medicines, and led the initial seed round in Menten.AI. From 2004 to 2017, he was editor in chief and publisher of MIT Technology Review. He has written for many publications, including The New York Times, Wired, and The Economist. In 2013, he delivered a TED talk entitled "Can technology solve our big problems?" which has been viewed more than 1.5 million times.

Andrew Zhu, MD/PhD

Dr. Andrew Zhu is a Professor of Medicine at Harvard Medical School, Director of Jiahui International Cancer Center (JICC), Director of JIH Clinical Research. Dr. Zhu is an internationally recognized leader in hepatocellular carcinoma (HCC) and cholangiocarcinoma, and has served as a principle investigator in many pivotal clinical trials in HCC, cholangiocarcinoma and other gastrointestinal cancers. As the lead global principal investigator, he led the pivotal studies which resulted in regulatory approval of pembrolizumab and ramucirumab in advanced HCC. As a co-principal investigator, he led the phase III trial of first IDH-1 inhibitor Ivosidenib in cholangiocarcinoma with IDH-1 mutations, which met the primary endpoint.

Wenle Xia, MD

Dr. Wenle Xia was former Chief Scientific Officer of Adlai Nortye, the Director of Translational Research Laboratory at Duke Cancer Institute and an Associate Professor in the Department of Medicine, head of GSK Oncology Translational Research and Chief Scientific Officer of Yangtze River Pharmaceutical Group Co., Ltd. Dr. Xia is well recognized for his contributions in the discovery and development ErbB targeted therapy and Lapatinib, which was approved by FDA in 2007.

Disclaimer: Participation by Dr. Evans and Dr. Hunter does not constitute or imply endorsement by the Salk Institute for Biological Studies.

About Adlai Nortye

Adlai Nortye is a global clinical-stage biopharmaceutical company with a highly differentiated immuno-oncology focused pipeline through global collaborations and internal discovery. The pipeline contains multiple preclinical and clinical stage drug candidates, and three of them are under clinical development, including the FDA Fast Track-designated Buparlisib (AN2025) in a global phase III clinical trial; the FDA Fast Track-designated intravenously-administered oncolytic virus Pelareorep (AN1004) to have completed a phase II clinical trial; and an oral EP4 antagonist (AN0025) with a completed phase 1b trial in a neoadjuvant setting in colon cancer and an ongoing phase 1b trial in combination with Merck's KEYTRUDA (pembrolizumab) in patients with advanced solid tumors. Adlai Nortye is headquartered in Hangzhou, China, with a R&D and global clinical operations center in New Jersey, USA. For more information, please visit: en.adlainortye.com.

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Zentalis Pharmaceuticals Announces Late-Breaker Oral Presentation on WEE1 Inhibitor, ZN-c3, at the AACR Annual Meeting 2021 – GlobeNewswire

NEW YORK and SAN DIEGO, March 10, 2021 (GLOBE NEWSWIRE) -- Zentalis Pharmaceuticals, Inc. (Nasdaq: ZNTL), a clinical-stage biopharmaceutical company focused on discovering and developing small molecule therapeutics targeting fundamental biological pathways of cancers, today announced that three abstracts have been accepted for presentation, including a late-breaker on its WEE1 inhibitor, ZN-c3, at the upcoming American Association for Cancer Research (AACR) Annual Meeting 2021. The meeting will be held virtually on April 10-15 and May 17-21, 2021.

The important data we are presenting at AACR supports the ability of our Integrated Discovery Engine to develop differentiated oncology therapeutic candidates across diverse cancer targets and types, commented Dr. Anthony Sun, Chairman and Chief Executive Officer of Zentalis Pharmaceuticals. We especially look forward to presenting clinical data from our ongoing Phase 1 monotherapy trial of our WEE1 inhibitor, ZN-c3, selected for a late-breaking session. In addition, results from two cell-based studies of ZN-c3, and our EGFR inhibitor, ZN-e4, demonstrated impressive selectivity and tolerability, which we believe positions these candidates to improve upon the constraints of existing products.

Late-Breaker Oral Presentation:

Title: Clinical activity of a single-agent ZN-c3, an oral WEE1 inhibitor, in a Phase 1 dose-escalation trial in patients with advanced solid tumors Session: Early Clinical Trials with New Anticancer Agents Presentation Number: CT016 Date/Time: Saturday, April 10, 2021 at 1:30 p.m. EDT

Poster Presentations:

Title: Discovery of ZN-c3, a potent Wee-1 inhibitor with a differentiated pharmacologic and kinase selectivity profile Session: Molecular and Cellular Biology / GeneticsAbstract ID: 1965Date/Time: Available starting on Saturday, April 10, 2021 at 8:30 a.m. EDT

Title: Discovery of ZN-e4, an irreversible EGFR-TKI with potent anti-tumor activity in EGFR mutant non-small-cell lung cancer Session: Oncogene Growth Factors and their ReceptorsAbstract ID: 2423Date/Time: Available starting on Saturday, April 10, 2021 at 8:30 a.m. EDT

The poster presentation abstracts are currently available on the AACR Annual Meeting 2021 website at http://www.aacr.org/meeting/aacr-annual-meeting-2021/.

About Zentalis

Zentalis Pharmaceuticals, Inc. is a clinical-stage biopharmaceutical company focused on discovering and developing small molecule therapeutics targeting fundamental biological pathways of cancers. The Company is developing a broad pipeline of potentially best-in-class oncology candidates, all internally discovered, which include ZN-c5, an oral selective estrogen receptor degrader (SERD) for ER+/HER2- breast cancer, ZN-c3, a WEE1 inhibitor for advanced solid tumors, ZN-d5, a BCL-2 inhibitor for hematologic malignancies, and ZN-e4, an EGFR inhibitor for non-small cell lung carcinoma (NSCLC). Zentalis has licensed ZN-c5, ZN-c3 and ZN-d5 to its majority-owned joint venture, Zentera Therapeutics, to develop and commercialize these candidates in China. Zentalis has operations in both New York and San Diego.

For more information, please visitwww.zentalis.com. Follow Zentalis on Twitter at@ZentalisPand on LinkedIn atwww.linkedin.com/company/zentalis-pharmaceuticals.

Forward-Looking Statements

This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. All statements contained in this press release that do not relate to matters of historical fact should be considered forward-looking statements, including without limitation statements regarding our expectations surrounding the development, potential, safety, efficacy, and regulatory and clinical progress of our product candidates in the Unites States and globally, plans and timing for the release of data from our clinical trials and preclinical studies, and our participation in upcoming events and presentations. These statements are neither promises nor guarantees, but involve known and unknown risks, uncertainties and other important factors that may cause our actual results, performance or achievements to be materially different from any future results, performance or achievements expressed or implied by the forward-looking statements, including, but not limited to, the following: the outbreak of the novel coronavirus disease, COVID-19, has adversely impacted and may continue to adversely impact our business, including our preclinical studies and clinical trials; our limited operating history, which may make it difficult to evaluate our current business and predict our future success and viability; we have and expect to continue to incur significant losses; our need for additional funding, which may not be available; our substantial dependence on the success of our lead product candidate; failure to identify additional product candidates and develop or commercialize marketable products; the early stage of our development efforts; potential unforeseen events during clinical trials could cause delays or other adverse consequences; risks relating to the regulatory approval process or ongoing regulatory obligations; failure to obtain U.S. or international marketing approval; our product candidates may cause serious adverse side effects; inability to maintain our collaborations, or the failure of these collaborations; our reliance on third parties; effects of significant competition; the possibility of system failures or security breaches; risks relating to intellectual property; our ability to attract, retain and motivate qualified personnel; and significant costs as a result of operating as a public company. These and other important factors discussed under the caption Risk Factors in our Quarterly Report on Form 10-Q for the quarterly period ended September 30, 2020 filed with the U.S. Securities and Exchange Commission (SEC) and our other filings with the SEC could cause actual results to differ materially from those indicated by the forward-looking statements made in this press release. Any such forward-looking statements represent managements estimates as of the date of this press release. While we may elect to update such forward-looking statements at some point in the future, we disclaim any obligation to do so, even if subsequent events cause our views to change.

Investor Contact:

Thomas HoffmannSolebury Trout1.646.378.2931thoffmann@soleburytrout.com

Media Contact:

Julia DeutschSolebury Trout1.646.378.2967jdeutsch@soleburytrout.com

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Zentalis Pharmaceuticals Announces Late-Breaker Oral Presentation on WEE1 Inhibitor, ZN-c3, at the AACR Annual Meeting 2021 - GlobeNewswire

Lipigon Expands Collaboration With HitGen by Selecting Second Target – BioSpace

CHENGDU, China--(BUSINESS WIRE)-- Lipigon AB (Lipigon), developer of therapeutics for lipid-related diseases, today announced that the company has expanded its agreement with the Shanghai STAR listed company HitGen Inc. (HitGen) to include a second novel target. With joint efforts, the aim is to develop a treatment for cardiometabolic disease.

Lipigon and HitGen have been collaborating on developing molecules enhancing lipoprotein lipase (LPL) activity since May 2020, with the aim to develop a novel drug for lipid disorders. Now the time is right to expand the collaboration by selecting a second undisclosed target.

Using HitGens proprietary DEL screening platform the parties will identify novel small molecules and jointly develop a candidate drug. Lipigon will be responsible for clinical development and out-licensing of commercialization rights of the drug candidates. HitGen is entitled to a starting fee and revenue sharing for any candidate resulting from the collaboration.

We are deeply impressed by the HitGen teams professionalism and hard work in the pre-screening activities of target 1 LPL. We are therefore pleased to expand our collaboration to include a second target, said Stefan K. Nilsson, CEO and co-founder of Lipigon. Target 2 is just as exciting as LPL and has a similarly strong genetic and clinical validation. HitGens world-leading screening platform will give us a good shot at finding relevant starting points for drug development.

HitGen is determined to help biology expert companies, such as Lipigon, finding new small-molecule leads where traditional screening has not been successful. We have a good track record of succeeding with difficult targets and with the input of Lipigon we hope to bring good lead candidates to the table, said Dr. Jin Li, Chairman of the Board and Chief Executive Officer of HitGen.

About Lipigon

Lipigon develops novel therapeutics for patients with lipid metabolism disorders. The company is based on over 50 years of lipid research at Ume University, Sweden. Lipigon's initial focus is on orphan drugs and niche indications, but in the long term, the company will have the opportunity to target broader indications in the area, such as diabetes and cardiovascular disease. Lipigons pipeline includes four active projects: the RNA-drug Lipisense, for treatment of hypertriglyceridemia; an RNA-drug for treatment of acute respiratory distress syndrome; a gene therapy treatment for the rare disease lipodystrophy, together with Combigene AB (publ); and a small molecule program for treatment of dyslipidemia in collaboration with HitGen (Inc).

The company's share (LPGO) is traded on the Nasdaq First North Growth Market. Certified Adviser is G&W Fondkommission, email: ca@gwkapital.se, phone: +46 8 503 000 50.

About HitGen Inc.

HitGen Inc. is a rapidly developing biotech company headquartered in Chengdu, China, with subsidiaries in Cambridge, UK and Houston, USA. It became a publicly listed company in Shanghai Stock Exchange in April 2020 (ticker code 688222.SH). HitGen has established a drug discovery research platform centered on the design, synthesis and screening of DNA encoded chemical libraries (DELs), fragment-based drug discovery (FBDD) and structure-based drug design (SBDD) technologies. HitGen's DELs currently contains more than 1 trillion novel, diverse, drug-like small molecules and macrocyclic compounds. These compounds are members of DELs synthesized from many hundreds of distinct chemical scaffolds, designed with tractable chemistry, and have yielded proven results for the discovery of small molecule leads against precedented and unprecedented classes of biological targets.

Through its acquisition of Cambridge UK based Vernalis R&D Ltd, a leader in FBDD/SBDD, HitGen now has a research team of over 500 scientists and offers a full set of research capabilities from recombinant protein expression and purification, structural biology, assay development, screening, DEL synthesis, nucleic acid and small molecule chemical synthesis, computational and medicinal chemistry, biochemistry and biophysics, cell biology, in vivo pharmacology, DMPK, CMC, etc., to enable drug discovery research from target gene to IND filing.

HitGen operates a flexible business model, ranging from a single capability-based fee for services (FFSe.g., protein expression and purification, structural biology, bioinformatics, computational chemistry, medicinal chemistry, nucleic and organic chemistry, analytical chemistry biophysics, PK, PD, etc.), DEL screening, DEL design, synthesis and characterization, integrated drug discovery projects, risk sharing projects, collaborative ventures to program out-licensing. HitGen has approximately 20 in-house drug discovery programs at different stages of research & development. HitGen is collaborating with pharmaceutical, biotech and chemical companies, foundations and research institutes in North America, Europe, Asia, Africa and Australia to enable the discovery and development of novel medicines and agrochemicals.

View source version on businesswire.com: https://www.businesswire.com/news/home/20210310005391/en/

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Lipigon Expands Collaboration With HitGen by Selecting Second Target - BioSpace

The Mystery of the Missing Energy in Singlet Fission Solar Cells Solved – SciTechDaily

Yuttapoom Puttisong, Senior Lecturer in the Department of Physics, Chemistry and Biology at Linkping University. Credit: Thor Balkhed

Competition between triplet pair formation and excimer-like recombination controls singlet fission yield.

The efficiency of solar cells can be increased by exploiting a phenomenon known as singlet fission. However, unexplained energy losses during the reaction have until now been a major problem. A research group led by scientists at Linkping University, Sweden, has discovered what happens during singlet fission and where the lost energy goes. The results have been published in the journal Cell Reports Physical Science.

Solar energy is one of the most important fossil-free and eco-friendly sustainable sources of electricity. The silicon-based solar cells currently in use can at most use approximately 33% of the energy in sunlight and convert it to electricity. This is because the packets of light, or photons, in the suns beams have an energy that is either too low to be absorbed by the solar cell, or too high, so that part of the energy is dissipated to waste heat. This maximum theoretical efficiency is known as the Shockley-Queisser limit. In practice, the efficiency of modern solar cells is 20-25%.

Diphenyl hexatriene (DPH) was used as singlet fission material in this study. Credit: Thor Balkhed

However, a phenomenon in molecular photophysics known as singlet fission can allow photons with higher energy to be used and converted to electricity without heat loss. In recent years, singlet fission has attracted increasing attention from scientists, and intense activity is underway to develop the optimal material. However, unexplained energy losses during singlet fission have until now made it difficult to design such a material. Researchers have not been able to agree on the origin of these energy losses.

Now, researchers at Linkping University, together with colleagues in Cambridge, Oxford, Donostia, and Barcelona, have discovered where the energy goes during singlet fission.

Singlet fission takes place in less than a nanosecond, and this makes it extremely difficult to measure. Our discovery allows us to open the black box and see where the energy goes during the reaction. In this way we will eventually be able to optimize the material to increase the efficiency of solar cells, says Yuttapoom Puttisong, senior lecturer in the Department of Physics, Chemistry and Biology at Linkping University.

View from the inside of the magneto-optic instrument that helps Yuttapoom Puttisong and his team to develop a protocol in searching for energy loss in singlet fission. Credit: Thor Balkhed

Part of the energy disappears in the form of an intermediate bright state, and this is a problem that must be solved to achieve efficient singlet fission. The discovery of where the energy goes is a major step on the way to significantly higher solar cell efficiency from the current 33% to over 40%.

The researchers used a refined magneto-optical transient method to identify the location of energy loss. This technique has unique advantages in that it can examine the fingerprint of the singlet fission reaction at a nanosecond timescale. A monoclinic crystal of a polyene, diphenyl hexatriene (DPH), was used in this study. However, this new technique can be used to study singlet fission in a broader material library. Yuqing Huang is a former doctoral student in the Department of Physics, Chemistry and Biology at Linkping University, and first author of the article now published in a newly established journal, Cell Reports Physical Science.

The actual singlet fission process takes place in the crystalline material. If we can optimize this material to retain as much as possible of the energy from the singlet fission, we will be significantly closer to application in practice. In addition, the singlet fission material is solution-processable, which makes it cheap to manufacture and suitable for integration with existing solar cell technology, says Yuqing Huang.

Reference: Competition between triplet pair formation and excimer-like recombination controls singlet fission yield by Yuqing Huang, Irina A. Buyanova, Chanakarn Phansa, Maria E. Sandoval-Salinas, David Casanova, William K. Myers, Neil C. Greenham, Akshay Rao, Weimin M. Chen and Yuttapoom Puttisong, 8 February 2021, Cell Reports Physical Science.DOI: 10.1016/j.xcrp.2021.100339

The research has been funded principally by the Swedish Research Council and the Knut and Alice Wallenberg Foundation.

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The Mystery of the Missing Energy in Singlet Fission Solar Cells Solved - SciTechDaily

Moderna Hires Harvard Stem Cell Researcher Jonathan Hoggatt as Director of Hematology: What You Need to Know – Benzinga

Moderna, Inc. (NASDAQ: MRNA), which shot to prominence with its coronavirus vaccine program, is beefing up its research and developmentteam.

What Happened: Jonathan Hoggatt, who was a principal faculty member at Harvard Stem Cell Institute, has joined Cambridge, Massachusetts-based Moderna as director of hematology, according to a Twitter post by the researcher.

He served as assistant professor at the Harvard Medical School's Hoggatt Lab, which works on tissue regeneration and stem cell biology, with a particular focus on translational research to enhance bone marrow transplantation.

Hoggatt has a master's degree in biology and a doctoral degree in hematology, and pursued apost-doctoral program in stem cell biology, his LinkedIn profile revealed.

Related Link: The Week Ahead In Biotech (Feb. 28-March 6): KemPharm, Gilead FDA Decisions and More Earnings

Why It's Important: After the resounding success with its coronavirus vaccine program, it's logical Moderna now turns its attention toward other programs.

The company has a rich pipeline, comprising investigational prophylactic vaccines against infectious diseases, secreted and cell therapeutic candidates, cancer vaccine candidates, regenerative therapeutic candidates and immuno-oncology candidates.

The immuno-oncology pipeline consists of two candidates, namely mRNA-2416 for lymphoma and a triplet candidate, codenamed mRNA-2752, both aimed at treating lymphoma and solid tumors.

The new appointment may be signaling Moderna's intent to focus on these candidates in a big way.

MRNA Price Action: In premarket trading Friday, Moderna shares were slipping 1.36% to $130.50.

Related Link: The Daily Biotech Pulse: Fulgent's Big Quarter, Gilead Awaits FDA Decision, Apellis Winds Up COVID-19 Study

(Moderna's Cambridge, Massachusetts offices; photo by Fletcher via WikimediaCommons)

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Moderna Hires Harvard Stem Cell Researcher Jonathan Hoggatt as Director of Hematology: What You Need to Know - Benzinga