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ProDOL:一种用于确定标记程度的通用方法,以优化染色和分子计数。

ProDOL: a general method to determine the degree of labeling for staining optimization and molecular counting.

机构信息

Institute of Cardiovascular Sciences, College of Medical and Dental Sciences, University of Birmingham, Birmingham, UK.

School of Chemistry, College of Engineering and Physical Sciences, University of Birmingham, Birmingham, UK.

出版信息

Nat Methods. 2024 Sep;21(9):1708-1715. doi: 10.1038/s41592-024-02376-6. Epub 2024 Aug 8.

Abstract

Determining the label to target ratio, also known as the degree of labeling (DOL), is crucial for quantitative fluorescence microscopy and a high DOL with minimal unspecific labeling is beneficial for fluorescence microscopy in general. Yet robust, versatile and easy-to-use tools for measuring cell-specific labeling efficiencies are not available. Here we present a DOL determination technique named protein-tag DOL (ProDOL), which enables fast quantification and optimization of protein-tag labeling. With ProDOL various factors affecting labeling efficiency, including substrate type, incubation time and concentration, as well as sample fixation and cell type can be easily assessed. We applied ProDOL to investigate how human immunodeficiency virus-1 pathogenesis factor Nef modulates CD4 T cell activation measuring total and activated copy numbers of the adapter protein SLP-76 in signaling microclusters. ProDOL proved to be a versatile and robust tool for labeling calibration, enabling determination of labeling efficiencies, optimization of strategies and quantification of protein stoichiometry.

摘要

确定标签与靶标之比,也称为标记程度(DOL),对于定量荧光显微镜至关重要,并且具有最小非特异性标记的高 DOL 通常有利于荧光显微镜。然而,目前还没有用于测量细胞特异性标记效率的强大、通用且易于使用的工具。在这里,我们提出了一种称为蛋白标签 DOL(ProDOL)的 DOL 测定技术,该技术可实现蛋白标签标记的快速定量和优化。使用 ProDOL,可以轻松评估影响标记效率的各种因素,包括底物类型、孵育时间和浓度,以及样品固定和细胞类型。我们应用 ProDOL 来研究人类免疫缺陷病毒-1 发病因子 Nef 如何调节 CD4 T 细胞激活,测量信号小簇中衔接蛋白 SLP-76 的总激活拷贝数。ProDOL 被证明是一种通用且强大的标记校准工具,可用于确定标记效率、优化策略和量化蛋白质化学计量。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5682/11399104/8ddb5d82e26e/41592_2024_2376_Fig1_HTML.jpg

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