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Related groups Liu lab Choudhary lab Fischer lab Researchers studying the role of proteins in health and disease use experimental tools that inactivate proteins, destroy them, or prevent them from being made in cells. The new study appears in Science. Paper cited Mercer JAM, et al. March 14, 2024.
TPD is a rapidly evolving therapeutic modality to degrade a disease-causing proteins, thereby eliminating their function specifically. 1 TPD is expected to challenge undruggable proteins, which are highly difficult to target by conventional small molecules. How does TPD work? Nature News.
Options for cell-based proteindegrader assays Interest is growing in the use of targeted-proteindegradation to induce the breakdown of disease-causing proteins after treatment with small molecule drugs.
Sygnature Discovery identifies potent SHP2 degrader compounds using its proprietary targetedproteindegrader platform, CHARMED, in collaboration with Japanese specialty chemical company, UBE Corporation. UBE Corporation: www.ube.com
I studied Natural Sciences at the University of Cambridge, where I was exposed to a range of disciplines from chemistry to physiology, specialising in my last year in biochemistry. Shortly after finishing my studies, I landed my first job in industry working on cell biology research for several disease indications.
CBTS Supergroup Meetings By Rose Circeo February 27, 2024 Breadcrumb Home Chembio-Therapeutics CBTS Supergroup Meetings Regular program meetings draw participants from many research communities to share cutting-edge research and brainstorm new project ideas in a wide variety of fields relevant to chemical biology and therapeutics science.
Promising future Molecular glues offer exciting opportunities for targetedproteindegradation and new ways to reach some of the estimated 85% of undruggable targets in the proteome. Conventional drug development has often focused on finding small molecules that fit the active site of a protein.
a leading biotechnology company developing small molecule therapeutics based on its proprietary uSMITE platform of targetedproteindegradation technology, today announced that the company’s internal program to develop selective degraders that target key proteins within the TRK family has been published by the Journal of Medicinal Chemistry.
(NYSE: PFE) today announced a global collaboration to develop and commercialize ARV-471, an investigational oral PROTAC® (PROteolysis TArgeting Chimera) estrogen receptor proteindegrader. The estrogen receptor is a well-known disease driver in most breast cancers. Chief Executive Officer at Arvinas.
Obtaining adequate drug exposure in the brain is key to treating CNS diseases effectively. Prodrugs Remain in “Proof-of-Concept” Stages Prodrug strategies for CNS deliver have also been applied with varying success , with the most famous example being L-Dopa for Parkinson’s disease. Figure 18.
The companies will receive priority admission or renewal for one year of lab bench space with access to core facilities at the MBC BioLabs life sciences incubator, including access to Amgen ‘s scientific experts and business leaders to help advance their scientific programs.
Therapeutic oligos, such as ASOs, siRNAs, and other mRNA-targeted therapeutics, have emerged as an exciting modality with the potential to address a variety of previously untreatable conditions. Freely accessible, high-quality science is critical for innovation,” added Dr Katja Herzog, Senior Project and Grant Manager, EU-OPENSCREEN.
Antibody-drug conjugates (ADCs) have been a groundbreaking approach to cancer treatment with their ability to deliver cytotoxic drugs directly to diseased cells while sparing healthy tissues. This targeted delivery allows enhanced therapeutic efficacy while reducing the harmful side effects commonly associated with traditional chemotherapy.
In part a reasonable and justified reaction to the over-hyped “big science project” platforms funded during the pandemic bubble, this sentiment needs to considered in the context of how the innovation pendulum swings back and forth over cycles. Today’s common refrain around “assets-in, platforms-out” is pervasive.
By Jonathan Montagu, CEO of HotSpot Therapeutics, as part of the From The Trenches feature of LifeSciVC In the perpetual and never-ending race by the healthcare sector to unearth new approaches and therapeutics to address disease, one area in which we are seeing novel innovation is in the targeting of transcription factors.
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