dc.contributor.author | Stains, Cliff I. | |
dc.contributor.author | Lukovic, Elvedin | |
dc.contributor.author | Imperiali, Barbara | |
dc.date.accessioned | 2012-03-22T15:22:03Z | |
dc.date.available | 2012-03-22T15:22:03Z | |
dc.date.issued | 2010-09 | |
dc.date.submitted | 2010-05 | |
dc.identifier.issn | 1554-8929 | |
dc.identifier.issn | 1554-8937 | |
dc.identifier.uri | http://hdl.handle.net/1721.1/69830 | |
dc.description.abstract | Recent efforts have identified the p38alpha Ser/Thr kinase as a potential target for the treatment of inflammatory diseases as well as non-small cell lung carcinoma. Despite the significance of p38alpha, no direct activity probe compatible with cell lysate analysis exists. Instead, proxies for kinase activation, such as phosphospecific antibodies, which do not distinguish between p38 isoforms, are often used. Our laboratory has recently developed a sulfonamido-oxine (Sox) fluorophore that undergoes a significant increase in fluorescence in response to phosphorylation at a proximal residue, allowing for real-time activity measurements. Herein we report the rational design of a p38alpha-selective chemosensor using this approach. We have validated the selectivity of this sensor using specific inhibitors and immunodepletions and show that p38α activity can be monitored in crude lysates from a variety of cell lines, allowing for the potential use of this sensor in both clinical and basic science research applications. | en_US |
dc.description.sponsorship | National Institutes of Health (U.S.) (NRSA Fellowship (F32GM085909) | en_US |
dc.description.sponsorship | National Institutes of Health (U.S.) (NIH Cell Migration Consortium (GM064346)) | en_US |
dc.language.iso | en_US | |
dc.publisher | American Chemical Society | en_US |
dc.relation.isversionof | http://dx.doi.org/10.1021/cb100230y | en_US |
dc.rights | Article is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use. | en_US |
dc.source | Prof. Imperiali via Erja Kajosalo | en_US |
dc.title | A p38alpha-Selective Chemosensor for use in Unfractionated Cell Lysates | en_US |
dc.title.alternative | A p38α-Selective Chemosensor for use in Unfractionated Cell Lysates | en_US |
dc.type | Article | en_US |
dc.identifier.citation | Stains, Cliff I., Elvedin Luković, and Barbara Imperiali. “A p38alpha-Selective Chemosensor for Use in Unfractionated Cell Lysates.” ACS Chemical Biology 6.1 (2011): 101–105. | en_US |
dc.contributor.department | Massachusetts Institute of Technology. Department of Biology | en_US |
dc.contributor.department | Massachusetts Institute of Technology. Department of Chemistry | en_US |
dc.contributor.approver | Imperiali, Barbara | |
dc.contributor.mitauthor | Imperiali, Barbara | |
dc.contributor.mitauthor | Lukovic, Elvedin | |
dc.contributor.mitauthor | Stains, Cliff I. | |
dc.relation.journal | ACS Chemical Biology | en_US |
dc.eprint.version | Author's final manuscript | en_US |
dc.type.uri | http://purl.org/eprint/type/JournalArticle | en_US |
eprint.status | http://purl.org/eprint/status/PeerReviewed | en_US |
dspace.orderedauthors | Stains, Cliff I.; Luković, Elvedin; Imperiali, Barbara | en |
dc.identifier.orcid | https://orcid.org/0000-0002-5749-7869 | |
mit.license | PUBLISHER_POLICY | en_US |
mit.metadata.status | Complete | |