A Method for Quantifying Molecular Interactions Using Stochastic Modelling and Super-Resolution Microscopy

被引:21
作者
Bermudez-Hernandez, Keria [1 ,2 ]
Keegan, Sarah [1 ,2 ]
Whelan, Donna R. [1 ]
Reid, Dylan A. [1 ]
Zagelbaum, Jennifer [1 ]
Yin, Yandong [1 ]
Ma, Sisi [2 ]
Rothenberg, Eli [1 ]
Fenyo, David [1 ,2 ]
机构
[1] NYU, Sch Med, Dept Biochem & Mol Pharmacol, New York, NY 10003 USA
[2] NYU, Sch Med, Inst Syst Genet, New York, NY 10003 USA
来源
SCIENTIFIC REPORTS | 2017年 / 7卷
基金
美国国家卫生研究院;
关键词
OPTICAL RECONSTRUCTION MICROSCOPY; FLUORESCENCE MICROSCOPY; COLOCALIZATION ANALYSIS; CLUSTER-ANALYSIS; PROTEIN HETEROGENEITY; SPATIAL-ORGANIZATION; SINGLE; GUIDE; PALM;
D O I
10.1038/s41598-017-14922-8
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
We introduce the Interaction Factor (IF), a measure for quantifying the interaction of molecular clusters in super-resolution microscopy images. The IF is robust in the sense that it is independent of cluster density, and it only depends on the extent of the pair-wise interaction between different types of molecular clusters in the image. The IF for a single or a collection of images is estimated by first using stochastic modelling where the locations of clusters in the images are repeatedly randomized to estimate the distribution of the overlaps between the clusters in the absence of interaction (IF = 0). Second, an analytical form of the relationship between IF and the overlap (which has the random overlap as its only parameter) is used to estimate the IF for the experimentally observed overlap. The advantage of IF compared to conventional methods to quantify interaction in microscopy images is that it is insensitive to changing cluster density and is an absolute measure of interaction, making the interpretation of experiments easier. We validate the IF method by using both simulated and experimental data and provide an ImageJ plugin for determining the IF of an image.
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页数:13
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