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利什曼原虫 Rab5a 的 GDP 结合态 GTPase 结构域的晶体结构。

Crystal structure of the GDP-bound GTPase domain of Rab5a from Leishmania donovani.

机构信息

Molecular and Structural Biology Division, CSIR - Central Drug Research Institute, Lucknow 226 031, India.

X-ray Crystallography Facility, National Institute of Immunology, New Delhi 110 067, India.

出版信息

Acta Crystallogr F Struct Biol Commun. 2020 Nov 1;76(Pt 11):544-556. doi: 10.1107/S2053230X20013722. Epub 2020 Oct 29.

Abstract

Eukaryotic Rab5s are highly conserved small GTPase-family proteins that are involved in the regulation of early endocytosis. Leishmania donovani Rab5a regulates the sorting of early endosomes that are involved in the uptake of essential nutrients through fluid-phase endocytosis. Here, the 1.80 Å resolution crystal structure of the N-terminal GTPase domain of L. donovani Rab5a in complex with GDP is presented. The crystal structure determination was enabled by the design of specific single-site mutations and two deletions that were made to stabilize the protein for previous NMR studies. The structure of LdRab5a shows the canonical GTPase fold, with a six-stranded central mixed β-sheet surrounded by five α-helices. The positions of the Switch I and Switch II loops confirm an open conformation, as expected in the absence of the γ-phosphate. However, in comparison to other GTP-bound and GDP-bound homologous proteins, the Switch I region traces a unique disposition in LdRab5a. One magnesium ion is bound to the protein at the GTP-binding site. Molecular-dynamics simulations indicate that the GDP-bound structure exhibits higher stability than the apo structure. The GDP-bound LdRab5a structure presented here will aid in efforts to unravel its interactions with its regulators, including the guanine nucleotide-exchange factor, and will lay the foundation for a structure-based search for specific inhibitors.

摘要

真核生物 Rab5s 是高度保守的小 GTPase 家族蛋白,参与早期内吞作用的调节。利什曼原虫 Rab5a 调节早期内体的分拣,这些内体参与通过液相等分子内吞作用摄取必需营养物质。本文呈现了与 GDP 结合的 L. donovani Rab5a 的 N 端 GTPase 结构域的 1.80Å分辨率晶体结构。该晶体结构的测定得益于特定的单点突变和两个缺失的设计,这些设计用于稳定蛋白质,以便进行之前的 NMR 研究。LdRab5a 的结构显示出典型的 GTPase 折叠,具有一个由六个残基组成的中央混合β-折叠,周围有五个α-螺旋。开关 I 和开关 II 环的位置证实了一个开放构象,这与预期的无γ-磷酸酯的情况一致。然而,与其他 GTP 结合和 GDP 结合的同源蛋白相比,开关 I 区域在 LdRab5a 中呈现出独特的排列。一个镁离子结合在 GTP 结合位点的蛋白质上。分子动力学模拟表明,GDP 结合结构比无配体结构更稳定。本文呈现的 GDP 结合的 LdRab5a 结构将有助于揭示其与调节因子(包括鸟嘌呤核苷酸交换因子)的相互作用,并为基于结构的特异性抑制剂搜索奠定基础。

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