Activity based probes for proteases: Applications to biomarker discovery, molecular imaging and drug screening

被引:91
作者
Fonovic, Marko
Bogyo, Matthew
机构
[1] Stanford Univ, Sch Med, Dept Pathol, Stanford, CA 94305 USA
[2] Jozef Stefan Inst, Dept Biochem & Mol Biol, SL-1000 Ljubljana, Slovenia
关键词
proteases; activity based probes; proteomics; biomarkers;
D O I
10.2174/138161207779313623
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Recent advances in global genomic and proteomic methods have lead to a greater understanding of how genes and proteins function in complex networks within a cell. One of the major limitations in these methodologies is their inability to provide information on the dynamic, post-translational regulation of enzymatic proteins. In particular proteases are often synthesized as inactive zymogens that need to be activated in order to carry out specific biological processes. Thus, methods that allow direct monitoring of protease activity in the context of a living cell or whole animal will be required to begin to understand the systems-wide functional roles of proteases. In this review, we discuss the development and applications of activity based probes (ABPs) to study proteases and their role in pathological processes. Specifically we focus on application of this technique for biomarker discovery, in vivo imaging and drug screening.
引用
收藏
页码:253 / 261
页数:9
相关论文
共 77 条
[41]   Discovering potent and selective reversible inhibitors of enzymes in complex proteomes [J].
Leung, D ;
Hardouin, C ;
Boger, DL ;
Cravatt, BF .
NATURE BIOTECHNOLOGY, 2003, 21 (06) :687-691
[42]   Structure of human methionine aminopeptidase-2 complexed with fumagillin [J].
Liu, SP ;
Widom, J ;
Kemp, CW ;
Crews, CM ;
Clardy, J .
SCIENCE, 1998, 282 (5392) :1324-1327
[43]   Activity-based protein profiling: The serine hydrolases [J].
Liu, YS ;
Patricelli, MP ;
Cravatt, BF .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (26) :14694-14699
[44]   Communication between the active sites and dimer interface of a herpesvirus protease revealed by a transition-state inhibitor [J].
Marnett, AB ;
Nomura, AM ;
Shimba, N ;
de Montellano, PRO ;
Craik, CS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (18) :6870-6875
[45]   THE IDENTIFICATION OF ACTIVE FORMS OF CYSTEINE PROTEINASES IN KIRSTEN-VIRUS-TRANSFORMED MOUSE FIBROBLASTS BY USE OF A SPECIFIC RADIOLABELED INHIBITOR [J].
MASON, RW ;
WILCOX, D ;
WIKSTROM, P ;
SHAW, EN .
BIOCHEMICAL JOURNAL, 1989, 257 (01) :125-129
[46]   Structure and function of fatty acid amide hydrolase [J].
McKinney, MK ;
Cravatt, BF .
ANNUAL REVIEW OF BIOCHEMISTRY, 2005, 74 :411-432
[47]   Genomes, phylogeny, and evolutionary systems biology [J].
Medina, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 :6630-6635
[48]   Global analysis of proteasomal substrate specificity using positional-scanning libraries of covalent inhibitors [J].
Nazif, T ;
Bogyo, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (06) :2967-2972
[49]   High-resolution functional proteomics by active-site peptide profiling [J].
Okerberg, ES ;
Wu, JY ;
Zhang, BH ;
Samii, B ;
Blackford, K ;
Winn, DT ;
Shreder, KR ;
Burbaum, JJ ;
Patricelli, MP .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (14) :4996-5001
[50]   Stable isotope labeling by amino acids in cell culture, SILAC, as a simple and accurate approach to expression proteomics [J].
Ong, SE ;
Blagoev, B ;
Kratchmarova, I ;
Kristensen, DB ;
Steen, H ;
Pandey, A ;
Mann, M .
MOLECULAR & CELLULAR PROTEOMICS, 2002, 1 (05) :376-386