Recent advances in protein tyrosine phosphatase detection using chemical probes = 화학탐침을 이용한 PTP 검출에 대한 최근 연구동향

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dc.contributor.authorK Lee-
dc.contributor.authorH J Kang-
dc.contributor.authorY Xia-
dc.contributor.authorSang Jeon Chung-
dc.date.accessioned2017-04-19T09:22:12Z-
dc.date.available2017-04-19T09:22:12Z-
dc.date.issued2011-
dc.identifier.issn1871-5206-
dc.identifier.uri10.2174/187152011794941208ko
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/10057-
dc.description.abstractProtein tyrosine phosphatases (PTPs) are key regulatory enzymes in signal transduction pathways and their aberrancy has been implicated in various diseases such as cancers, metabolic syndrome, and autoimmune disorders. In spite of its great importance, determination of the functional significance of PTPs remains a major challenge, and efficient methodologies are needed to specifically delineate PTP functions. Besides the strategy to use potent and selective PTP inhibitors to study the physiological roles of the enzymes, measurement of PTP activities using specific PTP substrates or activity-based probes (ABPs) has been reported. This review focused on the recent development of small molecular probes to detect PTP activities, consisting of five sub-categories: 1. Conventional fluorescent substrates; 2. Ratiometric fluorescent PTP substrates; 3. Fluorescence substrates with selectivity to a single PTP or a class of PTPs; 4. ABPs specific for PTPs; and 5. A real-time imaging of PTP-substrate complex using a small molecule PTP probe which, offers a measurement of a real-time activity of a certain PTP in cells.-
dc.publisherBentham Science Publ Ltd-
dc.titleRecent advances in protein tyrosine phosphatase detection using chemical probes = 화학탐침을 이용한 PTP 검출에 대한 최근 연구동향-
dc.title.alternativeRecent advances in protein tyrosine phosphatase detection using chemical probes-
dc.typeArticle-
dc.citation.titleAnti-Cancer Agents in Medicinal Chemistry-
dc.citation.number1-
dc.citation.endPage63-
dc.citation.startPage54-
dc.citation.volume11-
dc.contributor.affiliatedAuthorSang Jeon Chung-
dc.contributor.alternativeName이경-
dc.contributor.alternativeName강효진-
dc.contributor.alternativeNameXia-
dc.contributor.alternativeName정상전-
dc.identifier.bibliographicCitationAnti-Cancer Agents in Medicinal Chemistry, vol. 11, no. 1, pp. 54-63-
dc.identifier.doi10.2174/187152011794941208-
dc.subject.keyword2-fluoromethylphosphotyrosine (FMPT)-
dc.subject.keyword4-fluoromethylphenylphosphate (FMPP)-
dc.subject.keywordDiFMUP-
dc.subject.keywordDual-specificity PTP (DUSP)-
dc.subject.keywordForster resonance energy transfer (FRET)-
dc.subject.keywordIn-gel assay-
dc.subject.keywordPhosphotyrosine-
dc.subject.local2-fluoromethylphosphotyrosine (FMPT)-
dc.subject.local4-fluoromethylphenylphosphate (FMPP)-
dc.subject.localDiFMUP-
dc.subject.localDual-specificity PTP (DUSP)-
dc.subject.localForster resonance energy transfer-
dc.subject.localForster resonance energy transfer (FRET)-
dc.subject.localIn-gel assay-
dc.subject.localPhosphotyrosine-
dc.description.journalClassY-
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