Expanded dynamic range of fluorescent indicators for Ca2+ by circularly permuted yellow fluorescent proteins

被引:871
作者
Nagai, T
Yamada, S
Tominaga, T
Ichikawa, M
Miyawaki, A
机构
[1] RIKEN, Brain Sci Inst, Lab Cell Funct & Dynam, Adv Technol Dev Grp, Wako, Saitama 3510198, Japan
[2] RIKEN, Brain Sci Inst, Lab Brain Operat Devices, Wako, Saitama 3510198, Japan
[3] JST, PRESTO, Kawaguchi, Saitama 3510198, Japan
[4] Kyoto Univ, Inst Virus Res, Lab Signal Transduct, Kyoto 6068507, Japan
关键词
D O I
10.1073/pnas.0400417101
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Fluorescence resonance energy transfer (FRET) technology has been used to develop genetically encoded fluorescent indicators for various cellular functions. Although most indicators have cyan- and yellow-emitting fluorescent proteins (CFP and YFP) as FRET donor and acceptor, their poor dynamic range often prevents detection of subtle but significant signals. Here, we optimized the relative orientation of the two chromophores in the Ca2+ indicator, yellow cameleon (YC) by fusing YFP at different angles. We generated circularly permuted YFPs (cpYFPs) that showed efficient maturation and acid stability. One of the cpYFPs incorporated in YC absorbs a great amount of excited energy from CFP in its Ca2+-saturated form, thereby increasing the Ca2+-dependent change in the ratio of YFP/CFP by nearly 600%. Both in cultured cells and in the nervous system of transgenic mice, the new YC enables visualization of subcellular Ca2+ dynamics with better spatial and temporal resolution than before. Our study provides an important guide for the development and improvement of indicators using GFP-based FRET.
引用
收藏
页码:10554 / 10559
页数:6
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