4.4 Review

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

期刊

BMB REPORTS
卷 47, 期 3, 页码 149-157

出版社

KOREAN SOCIETY BIOCHEMISTRY & MOLECULAR BIOLOGY
DOI: 10.5483/BMBRep.2014.47.3.264

关键词

Activity-based protein profiling; Fluorescent imaging; Proteomics; Small molecule probes; Systems biology

资金

  1. KIST [2N24080-2Z03780]
  2. Converging Research Center Program through the Ministry of Science, ICT and Future Planning [2013K000340]
  3. Eco Innovation Technology Development Program of the Korea Ministry of Environment

向作者/读者索取更多资源

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.

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