Fluorescence Imaging Methods to Investigate Translation in Single Cells

被引:29
作者
Biswas, Jeetayu [1 ]
Liu, Yang [2 ]
Singer, Robert H. [1 ,3 ,4 ]
Wu, Bin [2 ]
机构
[1] Albert Einstein Coll Med, Dept Anat & Struct Biol, Bronx, NY 10461 USA
[2] Johns Hopkins Sch Med, Ctr Cell Dynam, Dept Biophys & Biophys Chem, Dept Neurosci, Baltimore, MD 21218 USA
[3] Albert Einstein Coll Med, Gruss Lipper Biophoton Ctr, Bronx, NY 10461 USA
[4] Howard Hughes Med Inst, Janelia Res Campus, Ashburn, VA 20147 USA
基金
美国国家卫生研究院;
关键词
NEWLY SYNTHESIZED PROTEINS; MESSENGER-RNA TRANSLATION; LOCAL TRANSLATION; GENE-EXPRESSION; LIVE CELLS; VISUALIZATION; MOLECULE; REVEALS; LOCALIZATION; DYNAMICS;
D O I
10.1101/cshperspect.a032722
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Translation is the fundamental biological process that converts the genetic information in messenger RNAs (mRNAs) into functional proteins. Translation regulation allows cells to control when, where, and how many proteins are synthesized. Much of what we know about translation comes from ensemble approaches that measure the average of many cells. The cellular and molecular heterogeneity in the regulation of translation remains largely elusive. Fluorescence microscopy allows interrogation of biological problems with single-molecule, single-cell sensitivity. In recent years, improved design of reagents and microscopy tools has led to improved spatial and temporal resolution of translation imaging. It is now possible to track global translation in specific subcellular compartments and follow the translation dynamics of single transcripts. Highlighted here is the recent progress in translation imaging with emphasis on in vivo translation dynamics. These tools will be invaluable to the study of translation regulation.
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页数:15
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