醋兰氮杆菌 Shethna 蛋白 II(FeSII)的晶体结构表明存在结构域互换。

IF 2.6 4区 生物学 Q2 BIOCHEMICAL RESEARCH METHODS
Burak V Kabasakal, Ciaran R McFarlane, Charles A R Cotton, Anna Schmidt, Andrea Kung, Lucas Lieber, James W Murray
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引用次数: 0

摘要

葡萄氮杆菌 FeSII 蛋白与氮酶 MoFe 蛋白和 Fe 蛋白形成抗氧复合物。FeSII 是一种肾上腺毒素型铁氧还蛋白,在溶液中形成二聚体。此前,该晶体结构已被解决[Schlesier 等人(2016 年),J. Am. Chem. Soc. 138, 239-247],不对称单元中有五个拷贝。其中一个拷贝是正常的肾上腺素多肽结构域,与其晶体对称伴侣形成二聚体。其他四个拷贝呈 "开放 "构象,环路外翻,暴露出 2Fe-2S 簇。开放构象和封闭构象分别被解释为氧化构象和还原构象,开放构象的巨大构象变化允许与氮酶结合。在此,我们以相同的晶体形式独立地解决了 FeSII 的结构问题。原子在单位晶胞中的位置与早先的报告相似。但是,对结构的解释却有所不同。开放 "构象被解释为结晶引起的结构域交换的产物。2Fe-2S 簇没有暴露在溶剂中,但在晶体中,其相互作用的螺旋被来自晶体对称伴侣的相同螺旋残基所取代。结构域交换是复杂的,因为它不同寻常地位于蛋白质的中间而不是末端,而且它产生的分子排列可以有多种解释。此外,还需要注意的是,晶体结构应根据整个晶体的内容而不是一个不对称单元来解释。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The crystal structure of Shethna protein II (FeSII) from Azotobacter vinelandii suggests a domain swap.

The Azotobacter vinelandii FeSII protein forms an oxygen-resistant complex with the nitrogenase MoFe and Fe proteins. FeSII is an adrenodoxin-type ferredoxin that forms a dimer in solution. Previously, the crystal structure was solved [Schlesier et al. (2016), J. Am. Chem. Soc. 138, 239-247] with five copies in the asymmetric unit. One copy is a normal adrenodoxin domain that forms a dimer with its crystallographic symmetry mate. The other four copies are in an `open' conformation with a loop flipped out exposing the 2Fe-2S cluster. The open and closed conformations were interpreted as oxidized and reduced, respectively, and the large conformational change in the open configuration allowed binding to nitrogenase. Here, the structure of FeSII was independently solved in the same crystal form. The positioning of the atoms in the unit cell is similar to the earlier report. However, the interpretation of the structure is different. The `open' conformation is interpreted as the product of a crystallization-induced domain swap. The 2Fe-2S cluster is not exposed to solvent, but in the crystal its interacting helix is replaced by the same helix residues from a crystal symmetry mate. The domain swap is complicated, as it is unusual in being in the middle of the protein rather than at a terminus, and it creates arrangements of molecules that can be interpreted in multiple ways. It is also cautioned that crystal structures should be interpreted in terms of the contents of the entire crystal rather than of one asymmetric unit.

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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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