Chen Yi, Guo Jia
Biodesign Institute & School of Molecular Sciences, Arizona State University, Tempe, Arizona 85287, United States.
ACS Meas Sci Au. 2022 Aug 17;2(4):296-303. doi: 10.1021/acsmeasuresciau.2c00011. Epub 2022 Apr 26.
The ability to profile a large number of different proteins in individual cells in their native cellular locations is critical to accelerate our understanding of normal cell physiology and disease pathogenesis. Bulk cell protein quantification masks the cell heterogeneity in complex biological systems, while conventional immunofluorescence or immunohistochemistry are limited by their low multiplexing capacity. Recent technological advances in multiplexed protein imaging approaches allow many distinct proteins to be analyzed in single cells in situ. These methods will bring new insights into various biological and biomedical fields, such as cell type and subtype classification, signaling network regulation, tissue architecture, and disease diagnosis and prognosis, along with treatment monitoring. In this Review, we will describe the recent advances of multiplexed single-cell in situ protein profiling technologies, discuss their unique advantages and limitations, highlight their applications in biology and medicine, present the current challenges, and propose potential solutions.
在单个细胞的天然细胞位置对大量不同蛋白质进行分析的能力,对于加速我们对正常细胞生理学和疾病发病机制的理解至关重要。大量细胞蛋白质定量掩盖了复杂生物系统中的细胞异质性,而传统的免疫荧光或免疫组织化学则受到其低多重分析能力的限制。多重蛋白质成像方法的最新技术进展允许在单细胞中原位分析许多不同的蛋白质。这些方法将为各种生物学和生物医学领域带来新的见解,如细胞类型和亚型分类、信号网络调节、组织结构以及疾病诊断和预后,以及治疗监测。在本综述中,我们将描述多重单细胞原位蛋白质分析技术的最新进展,讨论它们独特的优点和局限性,突出它们在生物学和医学中的应用,介绍当前的挑战,并提出潜在的解决方案。