Characterization of a conformationally sensitive TOAC spin-labeled substance P

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dc.contributor.authorShafer, Aaron M.
dc.contributor.authorNakaie, Clovis R. [UNIFESP]
dc.contributor.authorDeupi, Xavier
dc.contributor.authorBennett, Vicki J.
dc.contributor.authorVoss, John C.
dc.contributor.institutionUniv Calif Davis
dc.contributor.institutionNortheastern Ohio Univ Coll Med & Pharm
dc.contributor.institutionUniversidade Federal de São Paulo (UNIFESP)
dc.contributor.institutionUniv Autonoma Barcelona
dc.date.accessioned2016-01-24T13:51:52Z
dc.date.available2016-01-24T13:51:52Z
dc.date.issued2008-11-01
dc.description.abstractTo probe the binding of a peptide agonist to a G-protein coupled receptor in native membranes, the spin-labeled amino acid analogue 4-amino-4-carboxy-2,2,6,6-tetramethyl-piperidino-1-oxyl (TOAC) was substituted at either position 4 or 9 within the substance P peptide (RPKPQQFFGLM-NH2), a potent agonist of the neurokinin-1 receptor. the affinity of the 4-TOAC analog is comparable to the native peptide while the affinity of the 9-TOAC derivative is similar to 250-fold lower. Both peptides activate receptor signaling, though the potency of the 9-TOAC peptide is substantially lower. the utility of these modified ligands for reporting conformational dynamics during the neurokinin-1 receptor activation was explored using EPR spectroscopy, which can determine the real-time dynamics of the TOAC nitroxides in solution. While the binding of both the 4-TOAC substance P and 9-TOAC substance P peptides to isolated cell membranes containing the neurokinin-1 receptor is detected, a bound signal for the 9-TOAC peptide is only obtained under conditions that maintain the receptor in its high-affinity binding state. in contrast, 4-TOAC substance P binding is observed by solution EPR under both low- and high-affinity receptor states, with evidence of a more strongly immobilized peptide in the presence of GDP. in addition, to better understand the conformational consequences of TOAC substitution into substance P as it relates to receptor binding and activation, atomistic models for both the 4- and 9-TOAC versions of the peptide were constructed, and the molecular dynamics calculated via simulated annealing to explore the influence of the TOAC substitutions on backbone structure. (C) 2008 Elsevier Inc. All rights reserved.en
dc.description.affiliationUniv Calif Davis, Dept Biochem & Mol Med, Davis, CA 95616 USA
dc.description.affiliationNortheastern Ohio Univ Coll Med & Pharm, Dept Neurobiol & Pharmacol, Rootstown, OH 44272 USA
dc.description.affiliationUniversidade Federal de São Paulo, Escola Paulista Med, Dept Biofis, São Paulo, Brazil
dc.description.affiliationUniv Autonoma Barcelona, Sch Med, Biostat Unit, Lab Compuatat Med, Barcelona 08193, Catalunya, Spain
dc.description.affiliationUnifespUniversidade Federal de São Paulo, Escola Paulista Med, Dept Biofis, São Paulo, Brazil
dc.description.sourceWeb of Science
dc.description.sponsorshipNIH
dc.description.sponsorshipMinisterio de Educacion y Ciencia (Spain)
dc.description.sponsorshipIDNIH: NS25999
dc.description.sponsorshipID: C06 RR-12088-01
dc.format.extent1919-1929
dc.identifierhttp://dx.doi.org/10.1016/j.peptides.2008.08.002
dc.identifier.citationPeptides. New York: Elsevier B.V., v. 29, n. 11, p. 1919-1929, 2008.
dc.identifier.doi10.1016/j.peptides.2008.08.002
dc.identifier.issn0196-9781
dc.identifier.urihttp://repositorio.unifesp.br/handle/11600/31014
dc.identifier.wosWOS:000261023900009
dc.language.isoeng
dc.publisherElsevier B.V.
dc.relation.ispartofPeptides
dc.rightsinfo:eu-repo/semantics/restrictedAccess
dc.rights.licensehttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
dc.subjectSubstance Pen
dc.subjectGPCRen
dc.subjectTOAC spin labelen
dc.subjectEPRen
dc.subjectESRen
dc.titleCharacterization of a conformationally sensitive TOAC spin-labeled substance Pen
dc.typeinfo:eu-repo/semantics/article
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