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本文引用的文献

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Stoichiometry of molecular complexes at adhesions in living cells.活细胞中黏附处分子复合物的化学计量学。
Proc Natl Acad Sci U S A. 2009 Feb 17;106(7):2170-5. doi: 10.1073/pnas.0806036106. Epub 2009 Jan 23.
2
Detecting protein complexes in living cells from laser scanning confocal image sequences by the cross correlation raster image spectroscopy method.利用互相关光栅图像光谱法从激光扫描共聚焦图像序列中检测活细胞中的蛋白质复合物。
Biophys J. 2009 Jan;96(2):707-16. doi: 10.1016/j.bpj.2008.09.051.
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Annexin A2 binding to endosomes and functions in endosomal transport are regulated by tyrosine 23 phosphorylation.膜联蛋白A2与内体的结合及在内体运输中的功能受酪氨酸23磷酸化的调控。
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Annexin A8 regulates late endosome organization and function.膜联蛋白A8调节晚期内体的组织和功能。
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Accurate measurements of protein interactions in cells via improved spatial image cross-correlation spectroscopy.通过改进的空间图像互相关光谱法精确测量细胞中的蛋白质相互作用。
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6
Kinetics of morphogen gradient formation.形态发生素梯度形成的动力学
Science. 2007 Jan 26;315(5811):521-5. doi: 10.1126/science.1135774.
7
Particle image correlation spectroscopy (PICS): retrieving nanometer-scale correlations from high-density single-molecule position data.粒子图像相关光谱法(PICS):从高密度单分子位置数据中获取纳米级相关性。
Biophys J. 2007 Jan 15;92(2):613-21. doi: 10.1529/biophysj.106.092577. Epub 2006 Nov 3.
8
The endocytic pathway and formation of the Wingless morphogen gradient.内吞途径与无翅形态发生素梯度的形成。
Development. 2006 Jan;133(2):307-17. doi: 10.1242/dev.02197. Epub 2005 Dec 14.
9
Dpp gradient formation by dynamin-dependent endocytosis: receptor trafficking and the diffusion model.由发动蛋白依赖性内吞作用形成的Dpp梯度:受体运输与扩散模型
Development. 2004 Oct;131(19):4843-56. doi: 10.1242/dev.01335.
10
Localization accuracy in single-molecule microscopy.单分子显微镜中的定位精度。
Biophys J. 2004 Feb;86(2):1185-200. doi: 10.1016/S0006-3495(04)74193-4.

用粒子图像相关光谱(PICCS)定量生物相互作用。

Quantification of biological interactions with particle image cross-correlation spectroscopy (PICCS).

机构信息

Physics of Life Processes, Leiden Institute of Physics, Leiden University, Leiden, The Netherlands.

出版信息

Biophys J. 2011 Apr 6;100(7):1810-8. doi: 10.1016/j.bpj.2010.12.3746.

DOI:10.1016/j.bpj.2010.12.3746
PMID:21463595
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3072609/
Abstract

A multitude of biological processes that involve multiple interaction partners are observed by two-color microscopy. Here we describe an analysis method for the robust quantification of correlation between signals in different color channels: particle image cross-correlation spectroscopy (PICCS). The method, which exploits the superior positional accuracy obtained in single-object and single-molecule microscopy, can extract the correlation fraction and length scale. We applied PICCS to correlation measurements in living tissues. The morphogen Decapentaplegic (Dpp) was imaged in wing imaginal disks of fruit fly larvae and we quantified what fraction of early endosomes contained Dpp.

摘要

双色显微镜可观察到涉及多个相互作用伙伴的多种生物过程。在此,我们描述了一种用于稳健定量分析不同颜色通道信号之间相关性的分析方法:粒子图像互相关光谱学(PICCS)。该方法利用单物体和单分子显微镜获得的优越位置精度,可以提取相关分数和长度尺度。我们将 PICCS 应用于活体组织中的相关测量。在果蝇幼虫的翅膀成虫盘(wing imaginal disks)中,我们对形态发生素 Decapentaplegic(Dpp)进行了成像,并定量了早期内体中包含 Dpp 的部分。