Using peptidyl aldehydes in activity-based proteomics

被引:6
|
作者
Sabido, Eduard [1 ,2 ]
Tarrago, Teresa [2 ]
Giralt, Ernest [1 ,2 ]
机构
[1] Univ Barcelona, Dept Quim Organ, E-08028 Barcelona, Spain
[2] Inst Recerca Biomed, Barcelona 08028, Spain
关键词
Aldehydes; Peptides; Activity-based proteomics; Prolyl oligopeptidase; PROLYL ENDOPEPTIDASE INHIBITOR; ACTIVITY-BASED PROBES; REVERSIBLE COVALENT INHIBITORS; PROTEIN-TYROSINE PHOSPHATASES; SERINE HYDROLASE ACTIVITIES; SOLID-PHASE; ARGININE-VASOPRESSIN; SELECTIVE INHIBITORS; CHEMICAL PROTEOMICS; CYSTEINE PROTEASES;
D O I
10.1016/j.bmcl.2009.04.148
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The broad inhibitory spectrum of aldehydes and the possibility that amino acid residues modulate their specificity point to the potential of using peptidyl aldehydes as activity-based probes. Here, we establish the potential of peptidyl aldehydes in activity-based proteomics by synthesizing different probes and using them to specifically label a well-known serine protease in an activity-dependent manner. From our results, peptidyl aldehydes emerge as promising activity-based probes that enable multiple enzymatic-class detection by substrate recognition and can be used in diverse activity-based proteomics applications like protein identification and activity profiling. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3752 / 3755
页数:4
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