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靶向蛋白质降解工具:概述与未来展望

Targeted Protein Degradation Tools: Overview and Future Perspectives.

作者信息

Prozzillo Yuri, Fattorini Gaia, Santopietro Maria Virginia, Suglia Luigi, Ruggiero Alessandra, Ferreri Diego, Messina Giovanni

机构信息

Department of Biology and Biotechnology "Charles Darwin", Sapienza University of Rome, 00185 Rome, Italy.

Department of Clinical Infection, Microbiology and Immunology, Institute of Infection and Global Health, University of Liverpool, Liverpool L69 3BX, UK.

出版信息

Biology (Basel). 2020 Nov 26;9(12):421. doi: 10.3390/biology9120421.

Abstract

Targeted protein inactivation (TPI) is an elegant approach to investigate protein function and its role in the cellular landscape, overcoming limitations of genetic perturbation strategies. These systems act in a reversible manner and reduce off-target effects exceeding the limitations of CRISPR/Cas9 and RNA interference, respectively. Several TPI have been developed and wisely improved, including compartment delocalization tools and protein degradation systems. However, unlike chemical tools such as PROTACs (PROteolysis TArgeting Chimeras), which work in a wild-type genomic background, TPI technologies require adding an aminoacidic signal sequence (tag) to the protein of interest (POI). On the other hand, the design and optimization of PROTACs are very laborious and time-consuming. In this review, we focus on anchor-away, deGradFP, auxin-inducible degron (AID) and dTAG technologies and discuss their recent applications and advances. Finally, we propose nano-grad, a novel nanobody-based protein degradation tool, which specifically proteolyzes endogenous tag-free target protein.

摘要

靶向蛋白质失活(TPI)是一种研究蛋白质功能及其在细胞环境中作用的精妙方法,克服了基因扰动策略的局限性。这些系统以可逆方式起作用,分别减少了超出CRISPR/Cas9和RNA干扰局限性的脱靶效应。已经开发并明智地改进了几种TPI,包括区室离位工具和蛋白质降解系统。然而,与在野生型基因组背景下起作用的化学工具(如PROTAC,即蛋白酶靶向嵌合体)不同,TPI技术需要向目标蛋白(POI)添加一个氨基酸信号序列(标签)。另一方面,PROTAC的设计和优化非常费力且耗时。在本综述中,我们重点介绍锚定离开、降解荧光蛋白、生长素诱导降解结构域(AID)和dTAG技术,并讨论它们的最新应用和进展。最后,我们提出了纳米降解技术,这是一种基于新型纳米抗体的蛋白质降解工具,可特异性地蛋白水解内源性无标签靶蛋白。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8fd5/7761331/8a4feb7255c7/biology-09-00421-g001.jpg

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