31P NMR analysis of the DNA conformation induced by protein binding -: SRY/DNA complexes

被引:17
作者
Castagné, C
Murphy, EC
Gronenborn, AM
Delepierre, M
机构
[1] Inst Pasteur, Nucl Magnet Resonance Lab, CNRS, URA 1129, F-75724 Paris 15, France
[2] NIDDKD, Chem Phys Lab, NIH, Bethesda, MD 20892 USA
来源
EUROPEAN JOURNAL OF BIOCHEMISTRY | 2000年 / 267卷 / 04期
关键词
P-31-NMR; SRY protein; DNA-protein complex;
D O I
10.1046/j.1432-1327.2000.01124.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Complexes of the HMG box protein SRY with two duplexes of 8 and 14 base pairs have been studied by P-31 NMR and complete assignment of all phosphorus signals of the bound DNA duplexes are presented. While for the free DNA, all P-31 signals display Limited spectral dispersion (< 0.8 p.p.m.) for the bound duplexes, P-31 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 P-31-P-31 2D exchange experiments.
引用
收藏
页码:1223 / 1229
页数:7
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