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使用精确 NOE 进行蛋白质的立体专一性分配。

Stereospecific assignments in proteins using exact NOEs.

机构信息

Laboratory of Physical Chemistry, Swiss Federal Institute of Technology, 8093, Zurich, Switzerland.

出版信息

J Biomol NMR. 2013 Nov;57(3):211-8. doi: 10.1007/s10858-013-9780-4. Epub 2013 Oct 18.

Abstract

Recently developed methods to measure distances in proteins with high accuracy by "exact" nuclear Overhauser effects (eNOEs) make it possible to determine stereospecific assignments, which are particularly important to fully exploit the accuracy of the eNOE distance measurements. Stereospecific assignments are determined by comparing the eNOE-derived distances to protein structure bundles calculated without stereospecific assignments, or an independently determined crystal structure. The absolute and relative CYANA target function difference upon swapping the stereospecific assignment of a diastereotopic group yields the respective stereospecific assignment. We applied the method to the eNOE data set that has recently been obtained for the third immunoglobulin-binding domain of protein G (GB3). The 884 eNOEs provide relevant data for 47 of the total of 75 diastereotopic groups. Stereospecific assignments could be established for 45 diastereotopic groups (96 %) using the X-ray structure, or for 27 diastereotopic groups (57 %) using structures calculated with the eNOE data set without stereospecific assignments, all of which are in agreement with those determined previously. The latter case is relevant for structure determinations based on eNOEs. The accuracy of the eNOE distance measurements is crucial for making stereospecific assignments because applying the same method to the traditional NOE data set for GB3 with imprecise upper distance bounds yields only 13 correct stereospecific assignments using the X-ray structure or 2 correct stereospecific assignments using NMR structures calculated without stereospecific assignments.

摘要

最近开发的通过“精确”核奥弗豪瑟效应(eNOE)精确测量蛋白质中距离的方法,使得确定立体专一性分配成为可能,这对于充分利用 eNOE 距离测量的准确性尤为重要。立体专一性分配是通过将 eNOE 衍生的距离与未进行立体专一性分配的蛋白质结构束或独立确定的晶体结构进行比较来确定的。交换非对映体基团的立体专一性分配时,绝对和相对 CYANA 目标函数差异分别给出相应的立体专一性分配。我们将该方法应用于最近获得的蛋白 G(GB3)第三个免疫球蛋白结合域的 eNOE 数据集。884 个 eNOE 为总共 75 个非对映体基团中的 47 个提供了相关数据。使用 X 射线结构可以为 45 个非对映体基团(96%)建立立体专一性分配,或者使用没有立体专一性分配的 eNOE 数据集计算的结构为 27 个非对映体基团(57%)建立立体专一性分配,所有这些都与之前确定的一致。在后一种情况下,对于基于 eNOE 的结构确定是相关的。eNOE 距离测量的准确性对于确定立体专一性分配至关重要,因为将相同的方法应用于具有不精确上限距离的传统 GB3 NOE 数据集,使用 X 射线结构仅能得到 13 个正确的立体专一性分配,而使用没有立体专一性分配的 NMR 结构计算则只能得到 2 个正确的立体专一性分配。

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