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用第二种模式丰富蛋白水解靶向嵌合体:二比一更好。

Enriching Proteolysis Targeting Chimeras with a Second Modality: When Two Are Better Than One.

机构信息

Department of Pharmacy and Biotechnology, Alma Mater Studiorum - University of Bologna, Via Belmeloro 6, 40126 Bologna, Italy.

Department for Life Quality Studies, Alma Mater Studiorum - University of Bologna, Corso d'Augusto 237, 47921 Rimini, Italy.

出版信息

J Med Chem. 2022 Jul 28;65(14):9507-9530. doi: 10.1021/acs.jmedchem.2c00302. Epub 2022 Jul 11.

Abstract

Proteolysis targeting chimera (PROTAC)-mediated protein degradation has prompted a radical rethink and is at a crucial stage in driving a drug discovery transition. To fully harness the potential of this technology, a growing paradigm toward enriching PROTACs with other therapeutic modalities has been proposed. Could researchers successfully combine two modalities to yield PROTACs with an expanded profile? In this Perspective, we try to answer this question. We discuss how this possibility encompasses different approaches, leading to PROTACs, PROTACs, PROTAC , and and PROTACs. This possibility promises to further enhance PROTAC efficacy and selectivity, minimize side effects, and hit undruggable targets. While PROTACs have reached the clinical investigation stage, additional steps must be taken toward the translational development of PROTACs. A deeper and detailed understanding of the most critical challenges is required to fully exploit these opportunities and decisively enrich the PROTAC toolbox.

摘要

蛋白水解靶向嵌合体(PROTAC)介导的蛋白质降解引发了彻底的重新思考,目前正处于推动药物发现转变的关键阶段。为了充分利用这项技术的潜力,人们提出了一种将其他治疗模式与 PROTAC 相结合的日益增长的范例。研究人员能否成功地将两种模式结合起来,得到具有扩展特性的 PROTAC 呢?在这篇观点文章中,我们试图回答这个问题。我们讨论了这种可能性包含哪些不同的方法,从而产生了 PROTAC 、 PROTAC 、 PROTAC 、 PROTAC 和 PROTAC 。这种可能性有望进一步提高 PROTAC 的疗效和选择性,最小化副作用,并攻克不可成药的靶点。虽然 PROTAC 已经进入临床研究阶段,但还需要采取更多措施来推进 PROTAC 的转化开发。为了充分利用这些机会并果断丰富 PROTAC 工具包,需要更深入和详细地了解最关键的挑战。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e51/9340767/d5701554996c/jm2c00302_0001.jpg

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