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揭示超分辨率显微镜数据中隐藏的新特征。

Unraveling novel features hidden in superresolution microscopy data.

作者信息

Holcman David

机构信息

Ecole Normale Supérieure; Institute for Biology; IBENS; Group of Computational Biology and Applied Mathematics; Paris, France.

出版信息

Commun Integr Biol. 2013 May 1;6(3):e23893. doi: 10.4161/cib.23893.

DOI:10.4161/cib.23893
PMID:23710279
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3656019/
Abstract

Stochastic analysis of superresolution microscopy data obtained from receptor trafficking on neurons reveals novel organized molecular assembly generating long range forces. Would that have been possible with single particle tracking? How have we characterized these molecular assemblies?

摘要

对从神经元上受体运输获得的超分辨率显微镜数据进行随机分析,揭示了产生长程力的新型有组织分子组装。单粒子追踪能做到这一点吗?我们如何表征这些分子组装?

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本文引用的文献

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Heterogeneity of AMPA receptor trafficking and molecular interactions revealed by superresolution analysis of live cell imaging.活细胞成像的超分辨率分析揭示了 AMPA 受体转运和分子相互作用的异质性。
Proc Natl Acad Sci U S A. 2012 Oct 16;109(42):17052-7. doi: 10.1073/pnas.1204589109. Epub 2012 Oct 3.
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Paradigm shift of the plasma membrane concept from the two-dimensional continuum fluid to the partitioned fluid: high-speed single-molecule tracking of membrane molecules.质膜概念从二维连续流体到分区流体的范式转变:膜分子的高速单分子追踪
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