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

Authors
Lee, Jun-SeokYoo, Young-HwaYoon, Chang No
Issue Date
2014-03-31
Publisher
KOREAN SOCIETY BIOCHEMISTRY & MOLECULAR BIOLOGY
Citation
BMB REPORTS, v.47, no.3, pp.149 - 157
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.
Keywords
SPECTROMETRY-BASED PROTEOMICS; MASS-SPECTROMETRY; QUANTITATIVE PROTEOMICS; GEL-ELECTROPHORESIS; HUMAN GENOME; PROTEIN; IDENTIFICATION; INHIBITORS; DISCOVERY; CHEMISTRY; SPECTROMETRY-BASED PROTEOMICS; MASS-SPECTROMETRY; QUANTITATIVE PROTEOMICS; GEL-ELECTROPHORESIS; HUMAN GENOME; PROTEIN; IDENTIFICATION; INHIBITORS; DISCOVERY; CHEMISTRY; Activity-based protein profiling; Fluorescent imaging; Proteomics; Small molecule probes; Systems biology
ISSN
1976-6696
URI
https://pubs.kist.re.kr/handle/201004/126977
DOI
10.5483/BMBRep.2014.47.3.264
Appears in Collections:
KIST Article > 2014
Files in This Item:
There are no files associated with this item.
Export
RIS (EndNote)
XLS (Excel)
XML

qrcode

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

BROWSE