Please use this identifier to cite or link to this item: https://doi.org/10.1002/bip.20664
DC FieldValue
dc.titleActivity based fingerprinting of proteases using FRET peptides
dc.contributor.authorSun, H.
dc.contributor.authorPanicker, R.C.
dc.contributor.authorYao, S.Q.
dc.date.accessioned2014-06-23T05:54:29Z
dc.date.available2014-06-23T05:54:29Z
dc.date.issued2007
dc.identifier.citationSun, H., Panicker, R.C., Yao, S.Q. (2007). Activity based fingerprinting of proteases using FRET peptides. Biopolymers - Peptide Science Section 88 (2) : 141-149. ScholarBank@NUS Repository. https://doi.org/10.1002/bip.20664
dc.identifier.issn00063525
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/77393
dc.description.abstractWe have successfully developed a protease assay using fluorescence resonance energy transfer based peptide libraries, which allows not only general detection of enzymatic activities, but more importantly substrate fingerprinting of proteases from different classes. The method allows the generation of substrate fingerprints of a protease from both the nonprime and prime sites. Therefore, it is well suited for profiling of major metalloproteases such as thermolysin and MMPs. We envisage that this method will provide a useful tool in the emerging field of "Catalomics" for high-throughput studies of proteases. © 2007 Wiley Periodicals, Inc.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1002/bip.20664
dc.sourceScopus
dc.subjectActivity-based fingerprinting
dc.subjectCatalomics
dc.subjectEnzyme assay
dc.subjectFRET
dc.subjectPeptide
dc.subjectProtease
dc.typeConference Paper
dc.contributor.departmentCHEMISTRY
dc.description.doi10.1002/bip.20664
dc.description.sourcetitleBiopolymers - Peptide Science Section
dc.description.volume88
dc.description.issue2
dc.description.page141-149
dc.description.codenBPSSF
dc.identifier.isiut000245299000009
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