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当场捕获泛素缺陷:基于新型泛素的活性位点定向探针。

Catching a DUB in the act: novel ubiquitin-based active site directed probes.

作者信息

Ekkebus Reggy, Flierman Dennis, Geurink Paul P, Ovaa Huib

出版信息

Curr Opin Chem Biol. 2014 Dec;23:63-70. doi: 10.1016/j.cbpa.2014.10.005.

Abstract

Protein ubiquitylation is an important regulator of protein function, localization and half-life. It plays a key role in most cellular processes including immune signaling. Deregulation of this process is a major causative factor for many diseases. A major advancement in the identification and characterization of the enzymes that remove ubiquitin, deubiquitylases (DUBs) was made by the development of activity-based probes (ABPs). Recent advances in chemical protein synthesis and ligation methodology has yielded novel reagents for use in ubiquitylation research. We describe recent advances and discuss future directions in reagent development for studying DUBs.

摘要

蛋白质泛素化是蛋白质功能、定位和半衰期的重要调节因子。它在包括免疫信号传导在内的大多数细胞过程中发挥关键作用。该过程的失调是许多疾病的主要致病因素。基于活性的探针(ABP)的开发在去除泛素的酶(去泛素化酶,DUBs)的鉴定和表征方面取得了重大进展。化学蛋白质合成和连接方法的最新进展产生了用于泛素化研究的新型试剂。我们描述了最近的进展,并讨论了用于研究DUBs的试剂开发的未来方向。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/477b/7185813/11e114f9f069/gr1_lrg.jpg

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