Van Benschoten Andrew H, Afonine Pavel V, Terwilliger Thomas C, Wall Michael E, Jackson Colin J, Sauter Nicholas K, Adams Paul D, Urzhumtsev Alexandre, Fraser James S
Department of Bioengineering and Therapeutic Sciences, University of California San Francisco, San Francisco, CA 94158, USA.
Physical Biosciences Division, Lawrence Berkeley National Laboratory, Berkeley, CA 94720, USA.
Acta Crystallogr D Biol Crystallogr. 2015 Aug;71(Pt 8):1657-67. doi: 10.1107/S1399004715007415. Epub 2015 Jul 28.
Identifying the intramolecular motions of proteins and nucleic acids is a major challenge in macromolecular X-ray crystallography. Because Bragg diffraction describes the average positional distribution of crystalline atoms with imperfect precision, the resulting electron density can be compatible with multiple models of motion. Diffuse X-ray scattering can reduce this degeneracy by reporting on correlated atomic displacements. Although recent technological advances are increasing the potential to accurately measure diffuse scattering, computational modeling and validation tools are still needed to quantify the agreement between experimental data and different parameterizations of crystalline disorder. A new tool, phenix.diffuse, addresses this need by employing Guinier's equation to calculate diffuse scattering from Protein Data Bank (PDB)-formatted structural ensembles. As an example case, phenix.diffuse is applied to translation-libration-screw (TLS) refinement, which models rigid-body displacement for segments of the macromolecule. To enable the calculation of diffuse scattering from TLS-refined structures, phenix.tls_as_xyz builds multi-model PDB files that sample the underlying T, L and S tensors. In the glycerophosphodiesterase GpdQ, alternative TLS-group partitioning and different motional correlations between groups yield markedly dissimilar diffuse scattering maps with distinct implications for molecular mechanism and allostery. These methods demonstrate how, in principle, X-ray diffuse scattering could extend macromolecular structural refinement, validation and analysis.
识别蛋白质和核酸的分子内运动是大分子X射线晶体学中的一项重大挑战。由于布拉格衍射对晶体原子平均位置分布的描述精度欠佳,所得电子密度可能与多种运动模型相匹配。漫散射X射线可通过报告相关原子位移来减少这种简并性。尽管最近的技术进步提高了精确测量漫散射的可能性,但仍需要计算建模和验证工具来量化实验数据与晶体无序不同参数化之间的一致性。一种新工具phenix.diffuse通过采用吉尼尔方程来计算来自蛋白质数据库(PDB)格式结构集合的漫散射,满足了这一需求。作为一个示例,phenix.diffuse应用于平移-摆动-螺旋(TLS)精修,该方法对大分子片段的刚体位移进行建模。为了能够计算TLS精修结构的漫散射,phenix.tls_as_xyz构建了对基础T、L和S张量进行采样的多模型PDB文件。在甘油磷酸二酯酶GpdQ中,不同的TLS组划分以及组间不同的运动相关性会产生明显不同的漫散射图谱,对分子机制和变构效应具有不同的意义。这些方法表明,原则上X射线漫散射可以扩展大分子结构的精修、验证和分析。