Thread: NMR paper 31P NMR analysis of the DNA conformation induced by protein binding SRY/DNA complexes
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Default 31P NMR analysis of the DNA conformation induced by protein binding SRY/DNA complexes
31P NMR analysis of the DNA conformation induced by protein binding SRY/DNA complexes.

Related Articles 31P NMR analysis of the DNA conformation induced by protein binding SRY/DNA complexes.

Eur J Biochem. 2000 Feb;267(4):1223-9

Authors: Castagné C, Murphy EC, Gronenborn AM, Delepierre M

Complexes of the HMG box protein SRY with two duplexes of 8 and 14 base pairs have been studied by 31P NMR and complete assignment of all phosphorus signals of the bound DNA duplexes are presented. While for the free DNA, all 31P signals display limited spectral dispersion (< 0.8 p.p.m.) for the bound duplexes, 31P resonances are spread over 2 p.p.m. Based on the previously published 3D structure of hSRY-HMG, with the 8 mer it is demonstrated that the upfield shifted resonances correspond to the site of partial intercalation of an isoleucine side chain into the DNA. Moreover, the observation of significant difference in linewidths between the two duplexes allows to estimate lifetime of the complexes from 31P-31P 2D exchange experiments.

PMID: 10672034 [PubMed - indexed for MEDLINE]



Source: PubMed
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