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单细胞蛋白质免疫印迹法

Single-Cell Western Blotting.

作者信息

Sinkala Elly, Herr Amy E

机构信息

Department of Bioengineering, University of California Berkeley, 306 Stanley Hall MC 1762, Berkeley, CA, 94720-1762, USA.

出版信息

Methods Mol Biol. 2015;1346:1-9. doi: 10.1007/978-1-4939-2987-0_1.

Abstract

Little headway has been made in single cell protein analysis, aside from tools that rely solely on antibody-probe based detection (i.e., flow cytometry, immunocytochemistry), which are limited by low specificity and multiplexing capabilities. To address these protein analysis gaps, we have introduced a single-cell western blot (scWestern). The protein assay is capable of highly specific analysis by coupling antibody-based detection with a polyacrylamide gel electrophoresis (PAGE) protein separation. Cells are settled via gravity into polyacrylamide (PA) microwells, chemically lysed in the wells, and then subjected to PAGE through the walls of the microwells and into the surrounding PA gel. Over a thousand single-cell separations are performed simultaneously, and multiple protein targets of interest are investigated. After PAGE separation, photo-immobilization of all proteins to the gel allows for antibody probing and lends to the archival quality of the scWestern assay where new proteins targets can be investigated months after the initial separations are performed.

摘要

除了仅依赖基于抗体探针检测的工具(即流式细胞术、免疫细胞化学)外,单细胞蛋白质分析进展甚微,而这些工具受到低特异性和多重检测能力的限制。为了解决这些蛋白质分析方面的差距,我们引入了单细胞蛋白质印迹法(scWestern)。该蛋白质检测方法通过将基于抗体的检测与聚丙烯酰胺凝胶电泳(PAGE)蛋白质分离相结合,能够进行高度特异性分析。细胞通过重力沉降到聚丙烯酰胺(PA)微孔中,在孔中进行化学裂解,然后通过微孔壁进行PAGE并进入周围的PA凝胶中。同时进行超过一千次单细胞分离,并研究多个感兴趣的蛋白质靶点。在PAGE分离后,将所有蛋白质光固定到凝胶上,以便进行抗体探测,并赋予scWestern检测的存档质量,即在首次分离数月后仍可研究新的蛋白质靶点。

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