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核磁共振法测定同寡聚体结构的系统解决方案。

Systematic solution to homo-oligomeric structures determined by NMR.

作者信息

Martin Jeffrey W, Zhou Pei, Donald Bruce R

机构信息

Department of Computer Science, Duke University, Durham, North Carolina, 27708.

出版信息

Proteins. 2015 Apr;83(4):651-61. doi: 10.1002/prot.24768. Epub 2015 Feb 5.

Abstract

Protein structure determination by NMR has predominantly relied on simulated annealing-based conformational search for a converged fold using primarily distance constraints, including constraints derived from nuclear Overhauser effects, paramagnetic relaxation enhancement, and cysteine crosslinkings. Although there is no guarantee that the converged fold represents the global minimum of the conformational space, it is generally accepted that good convergence is synonymous to the global minimum. Here, we show such a criterion breaks down in the presence of large numbers of ambiguous constraints from NMR experiments on homo-oligomeric protein complexes. A systematic evaluation of the conformational solutions that satisfy the NMR constraints of a trimeric membrane protein, DAGK, reveals 9 distinct folds, including the reported NMR and crystal structures. This result highlights the fundamental limitation of global fold determination for homo-oligomeric proteins using ambiguous distance constraints and provides a systematic solution for exhaustive enumeration of all satisfying solutions.

摘要

通过核磁共振(NMR)确定蛋白质结构主要依赖于基于模拟退火的构象搜索,以使用主要包括源自核Overhauser效应、顺磁弛豫增强和半胱氨酸交联的距离约束来获得收敛的折叠结构。尽管不能保证收敛的折叠结构代表构象空间的全局最小值,但人们普遍认为良好的收敛等同于全局最小值。在此,我们表明,在对同源寡聚体蛋白复合物进行NMR实验存在大量模糊约束的情况下,这一标准不再适用。对满足三聚体膜蛋白DAGK的NMR约束的构象解决方案进行系统评估,发现了9种不同的折叠结构,包括已报道的NMR和晶体结构。这一结果突出了使用模糊距离约束确定同源寡聚体蛋白全局折叠的基本局限性,并为详尽枚举所有满足的解决方案提供了系统的方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f2a4/4568557/18388023d130/nihms720573f1.jpg

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