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利用中子大分子晶体学确定质子化状态目前存在哪些限制?

What are the current limits on determination of protonation state using neutron macromolecular crystallography?

作者信息

Liebschner Dorothee, Afonine Pavel V, Moriarty Nigel W, Adams Paul D

机构信息

Molecular Biophysics and Integrated Bioimaging Division, Lawrence Berkeley National Laboratory (LBNL), Berkeley, CA, United States.

Molecular Biophysics and Integrated Bioimaging Division, Lawrence Berkeley National Laboratory (LBNL), Berkeley, CA, United States.

出版信息

Methods Enzymol. 2020;634:225-255. doi: 10.1016/bs.mie.2020.01.008. Epub 2020 Feb 13.

Abstract

The rate of deposition of models determined by neutron diffraction, or a hybrid approach that combines X-ray and neutron diffraction, has increased in recent years. The benefit of neutron diffraction is that hydrogen atom (H) positions are detectable, allowing for the determination of protonation state and water molecule orientation. This study analyses all neutron models deposited in the Protein Data Bank to date, focusing on protonation state and properties of H (or deuterium, D) atoms as well as the details of water molecules. In particular, clashes and hydrogen bonds involving H or D atoms are investigated. As water molecules are typically the least reproducible part of a structural model, their positions in neutron models were compared to those in homologous high-resolution X-ray structures. For models determined by joint refinement against X-ray and neutron data, the water structure comparison was also carried out for models re-refined against the X-ray data alone. The homologues have generally fewer conserved water molecules where X-ray only was used and the positions of equivalent waters vary more than in the case of the hybrid X-ray model. As neutron diffraction data are generally less complete than X-ray data, the influence of neutron data completeness on nuclear density maps was also analyzed. We observe and discuss systematic map quality deterioration as result of data incompleteness.

摘要

近年来,通过中子衍射或结合X射线与中子衍射的混合方法确定的模型沉积速率有所提高。中子衍射的优势在于能够检测氢原子(H)的位置,从而确定质子化状态和水分子取向。本研究分析了迄今为止存于蛋白质数据库中的所有中子模型,重点关注质子化状态、H(或氘,D)原子的性质以及水分子的细节。特别地,对涉及H或D原子的冲突和氢键进行了研究。由于水分子通常是结构模型中重现性最差的部分,因此将中子模型中水分子的位置与同源高分辨率X射线结构中的位置进行了比较。对于通过联合X射线和中子数据精修确定的模型,还对仅针对X射线数据重新精修的模型进行了水结构比较。在仅使用X射线的情况下,同源物中保守水分子通常较少,且等效水的位置变化比混合X射线模型的情况更大。由于中子衍射数据通常不如X射线数据完整,因此还分析了中子数据完整性对核密度图的影响。我们观察并讨论了数据不完整导致的系统图谱质量下降情况。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad95/7571246/3a8f6ebfbcd6/nihms-1636584-f0001.jpg

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