Visualizing cytoskeleton dynamics in mammalian cells using a humanized variant of monomeric red fluorescent protein

被引:21
作者
Fischer, M
Haase, I
Wiesner, S
Müller-Taubenberger, A
机构
[1] Tech Univ Munich, Lehrstuhl Organ Chem & Biochem, D-85747 Garching, Germany
[2] Max Planck Inst Biochem, D-82152 Martinsried, Germany
关键词
actin cytoskeleton; codon usage; chondrocytes; fluorescent protein; monomeric RFP; mRFPruby; NIH; 3T3; synthetic gene;
D O I
10.1016/j.febslet.2006.03.082
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Fluorescent proteins are versatile tools for live cell imaging studies. In particular, recent progress was achieved in the development of monomeric red fluorescent proteins (mRFPs) that show improved properties in respect to maturation and intracellular fluorescence. mRFPmars, a red fluorescent protein designed especially for the use in Diciyostelium, proved to be a brilliant label for different cytoskeletal elements. Here we report on the synthesis of a humanized version of a monomeric RFP, mRFPruby, which differs in sequence from mRFPmars in four amino acids and has a codon usage that is optimized for the application in mammalian cells. In order to demonstrate the usefulness of this new mRFP variant, mRFPruby fused to P-actin was expressed in different mouse cell lines and used to visualize actin cytoskeleton dynamics by live cell microscopy. (c) 2006 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:2495 / 2502
页数:8
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