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小分子探针阐明蛋白质组学背景下的全局酶活性。

Small-molecule probes elucidate global enzyme activity in a proteomic context.

机构信息

Molecular Recognition Research Center, Korea Institute of Science and Technology (KIST), Seoul 136-791; University of Science and Technology, Daejeon 305-333, Korea.

Molecular Recognition Research Center, Korea Institute of Science and Technology (KIST), Seoul 136-791, Korea.

出版信息

BMB Rep. 2014 Mar;47(3):149-57. doi: 10.5483/bmbrep.2014.47.3.264.

Abstract

The recent dramatic improvements in high-resolution mass spectrometry (MS) have revolutionized the speed and scope of proteomic studies. Conventional MS-based proteomics methodologies allow global protein profiling based on expression levels. Although these techniques are promising, there are numerous biological activities yet to be unveiled, such as the dynamic regulation of enzyme activity. Chemical proteomics is an emerging field that extends these types proteomic profiling. In particular, activity-based protein profiling (ABPP) utilizes small-molecule probes to monitor enzyme activity directly in living intact subjects. In this mini-review, we summarize the unique roles of small-molecule probes in proteomics studies and highlight some recent examples in which this principle has been applied.

摘要

近年来,高分辨率质谱(MS)的显著改进彻底改变了蛋白质组学研究的速度和范围。基于常规 MS 的蛋白质组学方法可以根据表达水平进行全面的蛋白质组分析。尽管这些技术很有前途,但仍有许多生物学活性有待揭示,例如酶活性的动态调节。化学蛋白质组学是一个新兴领域,它扩展了这些类型的蛋白质组学分析。特别是,基于活性的蛋白质组学分析(ABPP)利用小分子探针直接在活体完整样本中监测酶活性。在这篇迷你综述中,我们总结了小分子探针在蛋白质组学研究中的独特作用,并强调了一些最近应用该原理的实例。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b4e9/4163878/b78e91b08896/BMB-47-149-g0001.jpg

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