Drug Discovery for Diseases with High Unmet Need Through Perturbation of Biomolecular Condensates

被引:0
|
作者
Eftekharzadeh, Bahareh [1 ]
Mayfield, Aislinn [1 ]
Kauffman, Michael G. [1 ]
Reilly, John F. [1 ]
机构
[1] Nereid Therapeut, 451 D St, Boston, MA 02210 USA
关键词
biomolecular condensates; phase separation; CoreletTM Technology; high throughput screening; drug discovery; PHASE-SEPARATION; LIQUID DROPLETS; TRANSITIONS;
D O I
10.1016/j.jmb.2024.168855
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Biomolecular condensates (BMCs), play significant roles in organizing cellular functions in the absence of membranes through phase separation events involving RNA, proteins, and RNA-protein complexes. These membrane-less organelles form dynamic multivalent weak interactions, often involving intrinsically disordered proteins or regions (IDPs/IDRs). However, the nature of these crucial interactions, how most of these organelles are organized and are functional, remains unknown. Aberrant condensates have been implicated in neurodegenerative diseases and various cancers, presenting novel therapeutic opportunities for small molecule condensate modulators. Recent advancements in optogenetic technologies, particularly Corelet, enable precise manipulation of BMC dynamics within living cells, facilitating high- throughput screening for small molecules that target these complex structures. By elucidating the molecular mechanisms governing BMC formation and function, this innovative approach holds promise to unlock therapeutic strategies against previously "undruggable" protein targets, paving the way for effective interventions in disease. (c) 2024 The Authors. Published by Elsevier Ltd. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
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页数:8
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