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使用条纹相机通过多光子荧光寿命成像显微镜对蛋白质-蛋白质相互作用进行定量成像。

Quantitative imaging of protein-protein interactions by multiphoton fluorescence lifetime imaging microscopy using a streak camera.

作者信息

Krishnan R V, Masuda A, Centonze V E, Herman B

机构信息

University of Texas Health Science Center, Department of Cellular and Structural Biology, 7703 Floyd Curl Drive, San Antonio, Texas 78229, USA.

出版信息

J Biomed Opt. 2003 Jul;8(3):362-7. doi: 10.1117/1.1577574.

Abstract

Fluorescence lifetime imaging microscopy (FLIM) using multiphoton excitation techniques is now finding an important place in quantitative imaging of protein-protein interactions and intracellular physiology. Recent developments in multiphoton FLIM methods are reviewed and a novel multiphoton FLIM system using a streak camera is described. An example of a typical application of the system is provided in which the fluorescence resonance energy transfer between a donor-acceptor pair of fluorescent proteins within a cellular specimen is measured.

摘要

使用多光子激发技术的荧光寿命成像显微镜(FLIM)目前在蛋白质-蛋白质相互作用和细胞内生理学的定量成像中占据重要地位。本文综述了多光子FLIM方法的最新进展,并描述了一种使用条纹相机的新型多光子FLIM系统。文中给出了该系统典型应用的一个例子,即测量细胞样本中一对荧光蛋白供体-受体之间的荧光共振能量转移。

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