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绿色或红色荧光蛋白(GFP或DsRed)连接蛋白在非肌肉细胞和肌肉细胞中的表达。

Expression of green or red fluorescent protein (GFP or DsRed) linked proteins in nonmuscle and muscle cells.

作者信息

Ayoob J C, Shaner N C, Sanger J W, Sanger J M

机构信息

Department of Cell and Developmental Biology, University of Pennsylvania, Philadelphia, PA 19104-6058, USA.

出版信息

Mol Biotechnol. 2001 Jan;17(1):65-71. doi: 10.1385/MB:17:1:65.

Abstract

The introduction of the green fluorescent protein (GFP) plasmids that allow proteins and peptides to be expressed with a fluorescent tag has had a major impact on the field of cell biology. It has enabled the dynamics of a wide variety of proteins to be analyzed that could not otherwise be detected in live cells. Transient transfections of muscle and nonmuscle cells with plasmids encoding various cytoskeletal proteins ligated to green fluorescent protein or Ds red protein allow changes in the cytoskeletal network to be studied in the same cell for time periods up to several days. With this approach, proteins that could not be purified and directly labeled with fluorescent dyes and microinjected into cells can now be expressed and visualized in a wide variety of cells. Procedures are presented for transfection of the nonmuscle cell, PtK2, and primary cultures of embryonic chick myocytes, and for studying the live transfected cells.

摘要

绿色荧光蛋白(GFP)质粒的引入使得蛋白质和肽能够与荧光标签一起表达,这对细胞生物学领域产生了重大影响。它使人们能够分析多种蛋白质的动态变化,而这些变化在活细胞中用其他方法是无法检测到的。用编码与绿色荧光蛋白或Ds红色蛋白连接的各种细胞骨架蛋白的质粒对肌肉细胞和非肌肉细胞进行瞬时转染,可以在同一细胞中研究长达数天的细胞骨架网络变化。通过这种方法,那些无法纯化并用荧光染料直接标记后显微注射到细胞中的蛋白质,现在可以在多种细胞中表达并可视化。本文介绍了非肌肉细胞PtK2和胚胎鸡心肌细胞原代培养物的转染程序,以及对活转染细胞的研究方法。

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