Center for Network Systems Biology, Department of Biochemistry, Boston University, MA, USA.
FEBS J. 2021 Dec;288(24):6990-7001. doi: 10.1111/febs.15685. Epub 2021 Jan 7.
The proteome of a human cell is partitioned within organelles, such as the nucleus, and other subcellular compartments, such as the cytoplasm, forming a myriad of membrane-bound and membrane-free ultrastructures. This compartmentalization allows discrete biochemical processes to occur efficiently in isolation, with relevant proteins localized to appropriate niches to fulfill their biological function(s). Proper delivery and dynamic exchange of proteins between compartments underlie the regulation of many cellular processes, such as cell signaling, division, and programmed cell death. To this end, cells deploy dedicated trafficking mechanisms to ensure correct protein localization, as mis-localization can result in pathology. In addition to trafficking, variation in the expression, modification, and physical associations of proteins within and between cells can result in biological heterogeneity, motivating the need for single-cell measurements. In this review, we introduce diverse platform technologies developed for subcellular proteomics and high-throughput systems biology, with the aim of providing mechanistic insights into fundamental cell biological processes underlying healthy and diseased states, and valuable public data resources. In contrast to the rapidly advancing field of single-cell genomics, the single-cell spatial proteomics toolbox remains in its infancy, but is poised to make considerable advances in the coming years.
人类细胞的蛋白质组被分配到细胞器(如细胞核)和其他亚细胞隔室(如细胞质)中,形成无数的膜结合和无膜的超微结构。这种区室化允许离散的生化过程在隔离状态下有效地发生,相关蛋白被定位到适当的小生境以发挥其生物学功能。蛋白质在隔室之间的正确传递和动态交换是许多细胞过程(如细胞信号转导、分裂和程序性细胞死亡)调节的基础。为此,细胞利用专门的运输机制来确保正确的蛋白质定位,因为定位错误可能导致病理学。除了运输之外,细胞内和细胞间蛋白质的表达、修饰和物理相互作用的变化会导致生物学异质性,这就需要进行单细胞测量。在这篇综述中,我们介绍了用于亚细胞蛋白质组学和高通量系统生物学的各种平台技术,旨在为健康和疾病状态下基本的细胞生物学过程提供机制上的见解,并提供有价值的公共数据资源。与单细胞基因组学这一快速发展的领域相比,单细胞空间蛋白质组学工具包仍处于起步阶段,但在未来几年有望取得重大进展。