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通过与 MAD 四溴对苯二甲酸共结晶简化蛋白质结构的重原子衍生物。

Simplified heavy-atom derivatization of protein structures via co-crystallization with the MAD tetragon tetrabromoterephthalic acid.

机构信息

School of Biological Sciences, The University of Adelaide, Adelaide, South Australia 5005, Australia.

Institute of Photonics and Advanced Sensing (IPAS), School of Biological Sciences, The University of Adelaide, Adelaide, South Australia 5005, Australia.

出版信息

Acta Crystallogr F Struct Biol Commun. 2021 May 1;77(Pt 5):156-162. doi: 10.1107/S2053230X21004052. Epub 2021 Apr 28.

Abstract

The phase problem is a persistent bottleneck that impedes the structure-determination pipeline and must be solved to obtain atomic resolution crystal structures of macromolecules. Although molecular replacement has become the predominant method of solving the phase problem, many scenarios still exist in which experimental phasing is needed. Here, a proof-of-concept study is presented that shows the efficacy of using tetrabromoterephthalic acid (B4C) as an experimental phasing compound. Incorporating B4C into the crystal lattice using co-crystallization, the crystal structure of hen egg-white lysozyme was solved using MAD phasing. The strong anomalous signal generated by its four Br atoms coupled with its compatibility with commonly used crystallization reagents render B4C an effective experimental phasing compound that can be used to overcome the phase problem.

摘要

相问题是阻碍结构测定管道的持续瓶颈,必须加以解决,才能获得大分子的原子分辨率晶体结构。虽然分子置换已成为解决相问题的主要方法,但仍有许多情况下需要进行实验相分析。本文提出了一项概念验证研究,表明使用四溴对苯二甲酸(B4C)作为实验相分析化合物的有效性。通过共结晶将 B4C 引入晶格中,使用 MAD 相分析解决了鸡卵清白溶菌酶的晶体结构。其四个 Br 原子产生的强异常信号与其与常用结晶试剂的相容性相结合,使 B4C 成为一种有效的实验相分析化合物,可用于克服相问题。

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本文引用的文献

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