Total Internal Reflection Fluorescence (TIRF) Microscopy of Chlamydomonas Flagella

被引:33
作者
Engel, Benjamin D. [1 ]
Lechtreck, Karl-Ferdinand [2 ]
Sakai, Tsuyoshi [3 ]
Ikebe, Mitsuo [3 ]
Witman, George B. [2 ]
Marshall, Wallace F. [1 ]
机构
[1] Univ Calif San Francisco, Dept Biochem & Biophys, San Francisco, CA 94158 USA
[2] Univ Massachusetts, Sch Med, Dept Cell Biol, Worcester, MA 01655 USA
[3] Univ Massachusetts, Sch Med, Dept Physiol, Worcester, MA 01655 USA
来源
CILIA: MODEL ORGANISMS AND INTRAFLAGELLAR TRANSPORT | 2009年 / 93卷
关键词
INTRAFLAGELLAR TRANSPORT IFT; CAENORHABDITIS-ELEGANS; FUNCTIONAL-ANALYSIS; PRIMARY CILIUM; PROTEIN; MOTILITY; REINHARDTII; TURNOVER; PARTICLES; COMPLEX;
D O I
10.1016/S0091-679X(08)93009-0
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The eukaryotic flagellum is host to a variety of dynamic behaviors, including flagellar beating, the motility of glycoproteins in the flagellar membrane, and intraflagellar transport (ITT), the bidirectional traffic of protein particles between the flagellar base and tip. ITT is of particular interest, as it plays integral roles in flagellar length control, cell signaling, development, and human disease. However, our ability to understand dynamic flagellar processes such as ITT is limited in large part by the fidelity with which we can image these behaviors in living cells. This chapter introduces the application of total internal reflection fluorescence (TIRT) microscopy to visualize the flagella of Chlamydomonas reinhardtii. The advantages and challenges of TIRF are discussed in comparison to confocal and differential interference contrast techniques. This chapter also reviews current ITT insights gleaned from TIRF microscopy of Chlamydomonas and provides an outlook on the future of the technique, with particular emphasis on combining TIRT with other emerging imaging technologies.
引用
收藏
页码:157 / +
页数:22
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