Three-dimensional NMR structure of the sixth ligand-binding module of the human LDL receptor: comparison of two adjacent modules with different ligand binding specificities

被引:13
作者
Clayton, D
Brereton, IM
Kroon, PA
Smith, R [1 ]
机构
[1] Univ Queensland, Dept Biochem, Brisbane, Qld 4072, Australia
[2] Univ Queensland, Ctr Magnet Resonance, Brisbane, Qld 4072, Australia
基金
英国医学研究理事会;
关键词
low-density lipoprotein receptor; ligand-binding domain; ligand specificity; surface property; nuclear magnetic resonance spectroscopy; three-dimensional structure;
D O I
10.1016/S0014-5793(00)01842-1
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
The sixth ligand-binding module of the low-density lipoprotein receptor contributes to the binding of apolipoprotein B100-containing lipoproteins. H-1 NMR spectroscopy, DYANA and X-PLOR structure calculations were used to determine that this module has a well defined structure with a backbone conformation similar to other modules. Structures from calculations that simulated the presence of a calcium ion showed increased resolution without large increases in energy, increased deviations from idealised geometry or violations of experimental constraints. Investigation of the surface properties of this module indicates there are significant differences from the fifth module, which binds apolipoprotein E-containing lipoproteins in addition to apolipoprotein B100-containing lipoproteins. (C) 2000 Federation of European Biochemical Societies. Published by Elsevier Science B.V. All rights reserved.
引用
收藏
页码:118 / 122
页数:5
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