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尼古丁 MATE 转运蛋白的晶体结构为其底物转运机制提供了深入了解。

Crystal structures of a nicotine MATE transporter provide insight into its mechanism of substrate transport.

机构信息

Nara Institute of Science and Technology, Ikoma, Japan.

出版信息

FEBS Lett. 2021 Jul;595(14):1902-1913. doi: 10.1002/1873-3468.14136. Epub 2021 Jun 16.

Abstract

A transporter of the multidrug and toxic compound extrusion (MATE) family, Nicotiana tabacum MATE2 (NtMATE2), is located in the vacuole membrane of the tobacco plant root and is involved in the transportation of nicotine, a secondary or specialized metabolic compound in Solanaceae. Here, we report the crystal structures of NtMATE2 in its outward-facing forms. The overall structure has a bilobate V-shape with pseudo-symmetrical assembly of the N- and C-lobes. In one crystal structure, the C-lobe cavity of NtMATE2 interacts with an unidentified molecule that may partially mimic a substrate. In addition, NtMATE2-specific conformational transitions imply that an unprecedented movement of the transmembrane α-helix 7 is related to the release of the substrate into the vacuolar lumen.

摘要

一种多药和毒性化合物外排(MATE)家族的转运蛋白,烟草 MATE2(NtMATE2),位于烟草植物根部的液泡膜中,参与运输尼古丁,这是茄科植物中的一种次生或特化代谢化合物。在这里,我们报告了 NtMATE2 向外开放构象的晶体结构。整体结构具有双叶 V 形,N 叶和 C 叶的假对称组装。在一个晶体结构中,NtMATE2 的 C 叶腔与一个可能部分模拟底物的未鉴定分子相互作用。此外,NtMATE2 特有的构象转变表明,跨膜α-螺旋 7 的前所未有的运动与底物释放到液泡腔有关。

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