A practical guide to evaluating colocalization in biological microscopy

被引:1530
作者
Dunn, Kenneth W. [1 ]
Kamocka, Malgorzata M. [1 ]
McDonald, John H. [2 ]
机构
[1] Indiana Univ, Div Nephrol, Dept Med, Med Ctr, Indianapolis, IN 46202 USA
[2] Univ Delaware, Dept Biol Sci, Newark, DE USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY | 2011年 / 300卷 / 04期
基金
美国国家卫生研究院;
关键词
digital image analysis; fluorescence microscopy; confocal microscopy; FLUORESCENCE MICROSCOPY; HEXOKINASE ASSOCIATION; COMPARTMENTS; MODULATION; ENDOSOMES; PROTEIN; MITOCHONDRIA; RECEPTORS; TRANSPORT; DISTINCT;
D O I
10.1152/ajpcell.00462.2010
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Dunn KW, Kamocka MM, McDonald JH. A practical guide to evaluating colocalization in biological microscopy. Am J Physiol Cell Physiol 300: C723-C742, 2011. First published January 5, 2011; doi:10.1152/ajpcell.00462.2010.-Fluorescence microscopy is one of the most powerful tools for elucidating the cellular functions of proteins and other molecules. In many cases, the function of a molecule can be inferred from its association with specific intracellular compartments or molecular complexes, which is typically determined by comparing the distribution of a fluorescently labeled version of the molecule with that of a second, complementarily labeled probe. Although arguably the most common application of fluorescence microscopy in biomedical research, studies evaluating the "colocalization" of two probes are seldom quantified, despite a diversity of image analysis tools that have been specifically developed for that purpose. Here we provide a guide to analyzing colocalization in cell biology studies, emphasizing practical application of quantitative tools that are now widely available in commercial and free image analysis software.
引用
收藏
页码:C723 / C742
页数:20
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