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Substrate Screening of Protein Kinases: Detection Methods and Combinatorial Peptide Libraries

Authors
Kim, M (Kim, Mira)Shin, DS (Shin, Dong-Sik)Kim, J (Kim, Jaehi)Lee, YS (Lee, Yoon-Sik)
Issue Date
Nov-2010
Publisher
JOHN WILEY SONS INC
Citation
BIOPOLYMERS, v.94, no.6, pp 753 - 762
Pages
10
Journal Title
BIOPOLYMERS
Volume
94
Number
6
Start Page
753
End Page
762
URI
https://scholarworks.sookmyung.ac.kr/handle/2020.sw.sookmyung/147973
DOI
10.1002/bip.21506
ISSN
0006-3525
1097-0282
Abstract
The study of protein kinases has become a matter of great importance in the development of new drugs for the treatment of diseases including cancer and inflammation Substrate screening is the first step in the fundamental investigation of protein kinases and the development of inhibitors for use in drug discovery Towards this goal, various studies have been reported regarding the development of phospho-peptide detection methods and the screening of phosphorylated peptide sites by protein kinases This review introduces the detection methods for phosphorylation events using the reagents with (gamma(32)P)ATP, ligand-linked ATP, phospho-peptide-specific antibodies and metal chelating compounds Chemical modification methods using p-elimination for the detection of phospho-Ser/Thr peptides are introduced as will In addition, the implementations of combinatorial peptide libraries for screening peptide substrates of protein kinases are discussed The phage display approach has been suggested as an alternative method of using synthetic peptides for screening the substrate specificities of protein kinase However, a solid phase assay using a peptide library-bound polymer resin or a peptide-arrayed glass chip is preferred for high throughput screening (FITS) (C) 2010 Wiley Periodicals, Inc Biopolymers (Pept Sci) 94 753-762,
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