Suppr超能文献

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。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验