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通过 hyperLOPIT 实现的弓形虫蛋白质组的全面亚细胞图谱为蛋白质功能提供了空间背景。

A Comprehensive Subcellular Atlas of the Toxoplasma Proteome via hyperLOPIT Provides Spatial Context for Protein Functions.

机构信息

Department of Biochemistry, University of Cambridge, Cambridge CB2 1QW, UK.

Department of Biochemistry, University of Cambridge, Cambridge CB2 1QW, UK.

出版信息

Cell Host Microbe. 2020 Nov 11;28(5):752-766.e9. doi: 10.1016/j.chom.2020.09.011. Epub 2020 Oct 13.

Abstract

Apicomplexan parasites cause major human disease and food insecurity. They owe their considerable success to highly specialized cell compartments and structures. These adaptations drive their recognition, nondestructive penetration, and elaborate reengineering of the host's cells to promote their growth, dissemination, and the countering of host defenses. The evolution of unique apicomplexan cellular compartments is concomitant with vast proteomic novelty. Consequently, half of apicomplexan proteins are unique and uncharacterized. Here, we determine the steady-state subcellular location of thousands of proteins simultaneously within the globally prevalent apicomplexan parasite Toxoplasma gondii. This provides unprecedented comprehensive molecular definition of these unicellular eukaryotes and their specialized compartments, and these data reveal the spatial organizations of protein expression and function, adaptation to hosts, and the underlying evolutionary trajectories of these pathogens.

摘要

顶复门寄生虫可引起重大人类疾病和粮食不安全。它们之所以取得如此大的成功,是因为它们具有高度特化的细胞区室和结构。这些适应性驱动了它们对宿主细胞的识别、非破坏性穿透以及精细的再工程化,以促进其生长、传播和抵御宿主防御。独特的顶复门细胞区室的进化伴随着巨大的蛋白质组新异性。因此,有一半的顶复门蛋白是独特的且尚未被描述的。在这里,我们在全球流行的顶复门寄生虫弓形虫中同时确定了数千种蛋白质的稳态亚细胞位置。这为这些单细胞真核生物及其特化区室提供了前所未有的全面分子定义,这些数据揭示了蛋白质表达和功能的空间组织、对宿主的适应以及这些病原体的潜在进化轨迹。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39e5/7670262/e8e5c5b9fa62/fx1.jpg

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