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光滑念珠菌质膜蛋白的冷冻电子断层扫描

Cryo-Electron Tomography of Candida glabrata Plasma Membrane Proteins.

作者信息

Jiménez-Ortigosa Cristina, Jiang Jennifer, Chen Muyuan, Kuang Xuyuan, Healey Kelley R, Castellano Paul, Boparai Nikpreet, Ludtke Steven J, Perlin David S, Dai Wei

机构信息

Hackensack Meridian Health-Center for Discovery and Innovation, 111 Ideation Way, Nutley, NJ 07110, USA.

Department of Cell Biology and Neuroscience, Rutgers, The State University of New Jersey, 604 Allison Road, Piscataway, NJ 08854, USA.

出版信息

J Fungi (Basel). 2021 Feb 6;7(2):120. doi: 10.3390/jof7020120.

Abstract

Fungal plasma membrane proteins have long been recognized as targets for the development of antifungal agents. Despite recent progress in experimental approaches and computational structural predictions, our knowledge of the structural dynamics and spatial distribution of these membrane proteins in the context of their native lipid environment remains limited. By applying cryo-electron tomography (cryoET) and subtomogram analysis, we aim to characterize the structural characteristics and spatial distribution of membrane proteins present in plasma membranes. This study has resulted in the identification of the membrane-embedded structure of the fungal H+-ATPase, Pma1. Tomograms of the plasma membrane revealed that Pma1 complexes are heterogeneously distributed as hexamers that cluster into distinct membrane microdomains. This study characterizes fungal membrane proteins in the native cellular landscape and highlights the unique potential of cryoET to advance our understanding of cellular biology and biological systems.

摘要

真菌质膜蛋白长期以来一直被视为抗真菌药物开发的靶点。尽管在实验方法和计算结构预测方面取得了最新进展,但我们对这些膜蛋白在其天然脂质环境中的结构动力学和空间分布的了解仍然有限。通过应用冷冻电子断层扫描(cryoET)和亚断层图分析,我们旨在表征质膜中存在的膜蛋白的结构特征和空间分布。这项研究已鉴定出真菌H + -ATP酶Pma1的膜嵌入结构。质膜的断层图显示,Pma1复合物以六聚体的形式异质分布,这些六聚体聚集形成不同的膜微区。这项研究在天然细胞环境中表征了真菌膜蛋白,并突出了cryoET在推进我们对细胞生物学和生物系统理解方面的独特潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f81f/7914498/70dd4041eb2b/jof-07-00120-g001.jpg

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