FUCCI-Red: a single-color cell cycle indicator for fluorescence lifetime imaging

被引:12
|
作者
Shirmanova, Marina V. [1 ]
Gorbachev, Dmitry A. [2 ]
Sarkisyan, Karen S. [3 ]
Parnes, Alina P. [3 ]
Gavrina, Alena I. [1 ]
Polozova, Anastasia V. [1 ]
Kovaleva, Tatyana F. [1 ]
Snopova, Ludmila B. [1 ]
Dudenkova, Varvara V. [1 ]
Zagaynova, Elena V. [1 ,4 ]
Lukyanov, Konstantin A. [2 ]
机构
[1] Privolzhsky Res Med Univ, Minin & Pozharsky Sq 10-1, Nizhnii Novgorod 603005, Russia
[2] Skolkovo Inst Sci & Technol, Ctr Life Sci, Bolshoy Blvd 30,Bld 1, Moscow 121205, Russia
[3] Shemyakin Ovchinnikov Inst Bioorgan Chem, Miklukho Maklaya 16-10, Moscow 117997, Russia
[4] Lobachevsky State Univ Nizhny Novgorod, Gagarin Ave 23, Nizhnii Novgorod 603950, Russia
基金
俄罗斯科学基金会;
关键词
Fluorescent proteins; Genetically encoded probes; Multiparameter in vivo imaging; Fluorescence lifetime; Cell cycle; Tumor model;
D O I
10.1007/s00018-020-03712-7
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 phase of the cell cycle determines numerous aspects of cancer cell behaviour including invasiveness, ability to migrate and responsiveness to cytotoxic drugs. To non-invasively monitor progression of cell cycle in vivo, a family of genetically encoded fluorescent indicators, FUCCI (fluorescent ubiquitination-based cell cycle indicator), has been developed. Existing versions of FUCCI are based on fluorescent proteins of two or more different colors fused to cell-cycle-dependent degradation motifs. Thus, FUCCI-expressing cells emit light of different colors in different phases providing a robust way to monitor cell cycle progression by fluorescence microscopy and flow cytometry but limiting the possibility to simultaneously visualize other markers. To overcome this limitation, we developed a single-color variant of FUCCI, called FUCCI-Red, which utilizes two red fluorescent proteins with distinct fluorescence lifetimes, mCherry and mKate2. Similarly to FUCCI, these proteins carry cell cycle-dependent degradation motifs to resolve G1 and S/G2/M phases. We showed utility of FUCCI-Red by visualizing cell cycle progression of cancer cells in 2D and 3D cultures and monitoring development of tumors in vivo by confocal and fluorescence lifetime imaging microscopy (FLIM). Single-channel registration and red-shifted spectra make FUCCI-Red sensor a promising instrument for multiparameter in vivo imaging applications, which was demonstrated by simultaneous detection of cellular metabolic state using endogenous fluorescence in the blue range.
引用
收藏
页码:3467 / 3476
页数:10
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