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荧光显微镜中分子计数的最新进展。

An update on molecular counting in fluorescence microscopy.

机构信息

College of Medical and Dental Sciences & School of Chemistry, University of Birmingham, Birmingham, UK; Centre of Membrane Proteins and Receptors (COMPARE), Universities of Birmingham and Nottingham, UK.

College of Medical and Dental Sciences & School of Chemistry, University of Birmingham, Birmingham, UK; Centre of Membrane Proteins and Receptors (COMPARE), Universities of Birmingham and Nottingham, UK.

出版信息

Int J Biochem Cell Biol. 2021 Jun;135:105978. doi: 10.1016/j.biocel.2021.105978. Epub 2021 Apr 15.

Abstract

Quantitative assessment of protein complexes, such as receptor clusters in the context of cellular signalling, has become a pressing objective in cell biology. The advancements in the field of single molecule fluorescence microscopy have led to different approaches for counting protein copy numbers in various cellular structures. This has resulted in an increasing interest in robust calibration protocols addressing photophysical properties of fluorescent labels and the effect of labelling efficiencies. Here, we want to give an update on recent methods for protein counting with a focus on novel calibration protocols. In this context, we discuss different types of calibration samples and identify some of the challenges arising in molecular counting experiments. Some recently published applications offer potential approaches to tackle these challenges.

摘要

定量评估蛋白质复合物,如细胞信号转导背景下的受体簇,已成为细胞生物学中的一个紧迫目标。单分子荧光显微镜领域的进展已经为在各种细胞结构中计数蛋白质拷贝数提供了不同的方法。这导致人们越来越关注稳健的校准协议,以解决荧光标记的光物理性质和标记效率的影响。在这里,我们希望更新最近用于蛋白质计数的方法,重点介绍新的校准协议。在这方面,我们讨论了不同类型的校准样本,并确定了分子计数实验中出现的一些挑战。一些最近发表的应用提供了潜在的方法来解决这些挑战。

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