Fluorescence Lifetime of Fluorescent Proteins as an Intracellular Environment Probe Sensing the Cell Cycle Progression

被引:42
|
作者
Pliss, Artem [2 ]
Zhao, Lingling [2 ]
Ohulchanskyy, Tymish Y. [2 ]
Qu, Junle [1 ]
Prasad, Paras N. [2 ]
机构
[1] Shenzhen Univ, Inst Optoelect, Minist Educ & Guangdong Prov, Key Lab Optoelect Devices & Syst, Shenzhen 518060, Guangdong, Peoples R China
[2] SUNY Buffalo, Inst Lasers Photon & Biophoton, Buffalo, NY 14260 USA
关键词
DNA-REPLICATION SITES; REFRACTIVE-INDEX; MONOMERIC RED; LIVING CELLS; ORGANIZATION; NUCLEUS; PH; MICROSCOPY; MOLECULES; DYNAMICS;
D O I
10.1021/cb300065w
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
The fluorescence lifetime of fluorescent proteins is affected by the concentration of solutes in a medium, in inverse correlation with local refractive index. In this paper, we introduce the concept of using this dependence to probe cellular molecular environment and its transformation during cellular processes. We employ the fluorescence lifetime of Green Fluorescent Protein and tdTomato Fluorescent Protein expressed in cultured cells and probe the changes in the local molecular environment during the cell cycle progression. We report that the longest fluorescence lifetimes occurred during mitosis. Following the cell division, the fluorescence lifetimes of these proteins were rapidly shortened. Furthermore the fluorescence lifetime of tdTomato in the nucleoplasm gradually increased throughout the span of S-phase and remained constantly long until the end of interphase. We interpret the observed fluorescence lifetime changes to be derived from changes in concentration of macromolecular solutes in the cell interior throughout cell cycle progression.
引用
收藏
页码:1385 / 1392
页数:8
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