Abstract:
:The field of biochemistry is currently faced with the enormous challenge of assigning functional significance to more than thirty thousand predicted protein products encoded by the human genome. In order to accomplish this daunting task, methods will be required that facilitate the global analysis of proteins in complex biological systems. Recently, methods have been described for simultaneously monitoring the activity of multiple enzymes in crude proteomes based on their reactivity with tagged chemical probes. These activity based probes (ABPs) have used either radiochemical or biotin/avidin-based detection methods to allow consolidated visualization of numerous enzyme activities. Here we report the synthesis and evaluation of fluorescent activity based probes for the serine hydrolase super-family of enzymes. The fluorescent methods detailed herein provide superior throughput, sensitivity, and quantitative accuracy when compared to previously described ABPs, and provide a straight-forward platform for high-throughput proteome analysis.
journal_name
Proteomicsjournal_title
Proteomicsauthors
Patricelli MP,Giang DK,Stamp LM,Burbaum JJdoi
10.1002/1615-9861(200109)1:9<1067::AID-PROT1067>3.subject
Has Abstractpub_date
2001-09-01 00:00:00pages
1067-71issue
9eissn
1615-9853issn
1615-9861journal_volume
1pub_type
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