lifeesoaks:一种分析蛋白质晶体中溶剂通道和浸泡实验障碍的工具。

IF 2.6 4区 生物学 Q2 BIOCHEMICAL RESEARCH METHODS
Jonathan Pletzer-Zelgert, Christiane Ehrt, Inken Fender, Axel Griewel, Florian Flachsenberg, Gerhard Klebe, Matthias Rarey
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引用次数: 0

摘要

由于蛋白质结构的复杂性,其相应的晶体排列通常包含大量的溶剂占用空间。这些区域允许一定程度的晶体内蛋白质的柔韧性和溶质的流动性。因此,无论何时对晶体内部的动力学感兴趣,了解溶剂型通道和腔体的几何形状都是必不可少的。特别是在基于结构的药物设计的浸泡实验中,配体必须能够穿过晶体溶剂通道并到达相应的结合口袋。筛分不成功有时归因于晶体填料的几何形状,但其根本原因往往难以理解。这项工作提出了LifeSoaks,一种分析和可视化蛋白质晶体中溶剂通道的新工具。LifeSoaks使用基于Voronoi图的周期通道表示,可以有效地计算。通道瓶颈的大小和位置可能会阻碍分子扩散,可以直接从这个表示中得出。这项工作提出了PDB中所有晶体结构的计算瓶颈半径,并分析了通过浸泡实验获得的新的手工编制的结构数据集。结果表明,考虑瓶颈半径和通道目视检查有利于规划浸泡试验。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

LifeSoaks: a tool for analyzing solvent channels in protein crystals and obstacles for soaking experiments.

LifeSoaks: a tool for analyzing solvent channels in protein crystals and obstacles for soaking experiments.

LifeSoaks: a tool for analyzing solvent channels in protein crystals and obstacles for soaking experiments.

LifeSoaks: a tool for analyzing solvent channels in protein crystals and obstacles for soaking experiments.

Due to the structural complexity of proteins, their corresponding crystal arrangements generally contain a significant amount of solvent-occupied space. These areas allow a certain degree of intracrystalline protein flexibility and mobility of solutes. Therefore, knowledge of the geometry of solvent-filled channels and cavities is essential whenever the dynamics inside a crystal are of interest. Especially in soaking experiments for structure-based drug design, ligands must be able to traverse the crystal solvent channels and reach the corresponding binding pockets. Unsuccessful screenings are sometimes attributed to the geometry of the crystal packing, but the underlying causes are often difficult to understand. This work presents LifeSoaks, a novel tool for analyzing and visualizing solvent channels in protein crystals. LifeSoaks uses a Voronoi diagram-based periodic channel representation which can be efficiently computed. The size and location of channel bottlenecks, which might hinder molecular diffusion, can be directly derived from this representation. This work presents the calculated bottleneck radii for all crystal structures in the PDB and the analysis of a new, hand-curated data set of structures obtained by soaking experiments. The results indicate that the consideration of bottleneck radii and the visual inspection of channels are beneficial for planning soaking experiments.

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来源期刊
Acta Crystallographica. Section D, Structural Biology
Acta Crystallographica. Section D, Structural Biology BIOCHEMICAL RESEARCH METHODSBIOCHEMISTRY &-BIOCHEMISTRY & MOLECULAR BIOLOGY
CiteScore
4.50
自引率
13.60%
发文量
216
期刊介绍: Acta Crystallographica Section D welcomes the submission of articles covering any aspect of structural biology, with a particular emphasis on the structures of biological macromolecules or the methods used to determine them. Reports on new structures of biological importance may address the smallest macromolecules to the largest complex molecular machines. These structures may have been determined using any structural biology technique including crystallography, NMR, cryoEM and/or other techniques. The key criterion is that such articles must present significant new insights into biological, chemical or medical sciences. The inclusion of complementary data that support the conclusions drawn from the structural studies (such as binding studies, mass spectrometry, enzyme assays, or analysis of mutants or other modified forms of biological macromolecule) is encouraged. Methods articles may include new approaches to any aspect of biological structure determination or structure analysis but will only be accepted where they focus on new methods that are demonstrated to be of general applicability and importance to structural biology. Articles describing particularly difficult problems in structural biology are also welcomed, if the analysis would provide useful insights to others facing similar problems.
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