配体结合时的构象转变:从apo 构象预测全酶结构。

Conformational transitions upon ligand binding: holo-structure prediction from apo conformations.

机构信息

Computational Biomolecular Dynamics Group, Max-Planck-Institute for Biophysical Chemistry, Göttingen, Germany.

出版信息

PLoS Comput Biol. 2010 Jan;6(1):e1000634. doi: 10.1371/journal.pcbi.1000634. Epub 2010 Jan 8.

Abstract

Biological function of proteins is frequently associated with the formation of complexes with small-molecule ligands. Experimental structure determination of such complexes at atomic resolution, however, can be time-consuming and costly. Computational methods for structure prediction of protein/ligand complexes, particularly docking, are as yet restricted by their limited consideration of receptor flexibility, rendering them not applicable for predicting protein/ligand complexes if large conformational changes of the receptor upon ligand binding are involved. Accurate receptor models in the ligand-bound state (holo structures), however, are a prerequisite for successful structure-based drug design. Hence, if only an unbound (apo) structure is available distinct from the ligand-bound conformation, structure-based drug design is severely limited. We present a method to predict the structure of protein/ligand complexes based solely on the apo structure, the ligand and the radius of gyration of the holo structure. The method is applied to ten cases in which proteins undergo structural rearrangements of up to 7.1 A backbone RMSD upon ligand binding. In all cases, receptor models within 1.6 A backbone RMSD to the target were predicted and close-to-native ligand binding poses were obtained for 8 of 10 cases in the top-ranked complex models. A protocol is presented that is expected to enable structure modeling of protein/ligand complexes and structure-based drug design for cases where crystal structures of ligand-bound conformations are not available.

摘要

蛋白质的生物学功能通常与其与小分子配体形成复合物有关。然而,这种复合物的原子分辨率实验结构测定可能既耗时又昂贵。用于预测蛋白质/配体复合物结构的计算方法,特别是对接,由于受体灵活性考虑有限,其应用受到限制,如果涉及受体结合配体时的大构象变化,则无法用于预测蛋白质/配体复合物。然而,配体结合状态(完整结构)下的准确受体模型是成功进行基于结构的药物设计的前提条件。因此,如果仅提供与配体结合构象不同的无配体(apo)结构,则基于结构的药物设计将受到严重限制。我们提出了一种仅基于 apo 结构、配体和完整结构的回转半径来预测蛋白质/配体复合物结构的方法。该方法应用于 10 个案例,其中蛋白质在配体结合时发生了高达 7.1Å 后骨架 RMSD 的结构重排。在所有情况下,都预测了与靶标后骨架 RMSD 为 1.6Å 的受体模型,并在排名最高的复合物模型中,有 8 个案例获得了接近天然的配体结合构象。提出了一种方案,预计可用于那些无法获得配体结合构象晶体结构的蛋白质/配体复合物的结构建模和基于结构的药物设计。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9676/2796265/44d78d3de8fc/pcbi.1000634.g001.jpg

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