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人 ABC 转运蛋白的结构与机制。

Structure and Mechanism of Human ABC Transporters.

机构信息

The Hormel Institute, University of Minnesota, Austin, Minnesota, USA.

Institute of Molecular Biology and Biophysics, ETH Zurich, Switzerland; email:

出版信息

Annu Rev Biophys. 2023 May 9;52:275-300. doi: 10.1146/annurev-biophys-111622-091232. Epub 2023 Feb 3.

Abstract

ABC transporters are essential for cellular physiology. Humans have 48 ABC genes organized into seven distinct families. Of these genes, 44 (in five distinct families) encode for membrane transporters, of which several are involved in drug resistance and disease pathways resulting from transporter dysfunction. Over the last decade, advances in structural biology have vastly expanded our mechanistic understanding of human ABC transporter function, revealing details of their molecular arrangement, regulation, and interactions, facilitated in large part by advances in cryo-EM that have rendered hitherto inaccessible targets amenable to high-resolution structural analysis. As a result, experimentally determined structures of multiple members of each of the five families of ABC transporters in humans are now available. Here we review this recent progress, highlighting the physiological relevance of human ABC transporters and mechanistic insights gleaned from their direct structure determination. We also discuss the impact and limitations of model systems and structure prediction methods in understanding human ABC transporters and discuss current challenges and future research directions.

摘要

ABC 转运蛋白对于细胞生理学至关重要。人类有 48 个 ABC 基因,分为七个不同的家族。这些基因中,有 44 个(分布在五个不同的家族中)编码膜转运蛋白,其中一些与药物耐药性和转运蛋白功能障碍导致的疾病途径有关。在过去的十年中,结构生物学的进步极大地扩展了我们对人类 ABC 转运蛋白功能的机制理解,揭示了它们的分子排列、调节和相互作用的细节,这在很大程度上得益于 cryo-EM 的进步,这些进步使得以前无法接近的靶标能够进行高分辨率结构分析。因此,现在已经可以获得人类五个 ABC 转运蛋白家族中多个成员的实验确定结构。在这里,我们回顾了这一最新进展,强调了人类 ABC 转运蛋白的生理相关性以及从其直接结构测定中获得的机制见解。我们还讨论了模型系统和结构预测方法在理解人类 ABC 转运蛋白方面的影响和局限性,并讨论了当前的挑战和未来的研究方向。

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