jYCaMP: an optimized calcium indicator for two-photon imaging at fiber laser wavelengths

被引:49
|
作者
Mohr, Manuel Alexander [1 ,2 ,7 ]
Bushey, Daniel [1 ]
Aggarwal, Abhi [1 ,3 ]
Marvin, Jonathan S. [1 ]
Kim, Jeong Jun [1 ]
Marquez, Emiliano Jimenez [1 ,4 ]
Liang, Yajie [1 ,5 ]
Patel, Ronak [1 ]
Macklin, John J. [1 ]
Le, Chi-Yu [1 ]
Tsang, Arthur [1 ,5 ]
Tsegaye, Getahun [1 ,5 ]
Ahrens, Allison M. [6 ]
Chen, Jerry L. [6 ]
Kim, Douglas S. [1 ,5 ]
Wong, Allan M. [1 ,5 ]
Looge, Loren L. [1 ,5 ]
Schreiter, Eric R. [1 ,5 ]
Podgorski, Kaspar [1 ]
机构
[1] Janelia Res Campus, Howard Hughes Med Inst, Ashburn, VA 20147 USA
[2] Eidgenoss TH Zurich, Dept Biosyst Sci & Engn, Basel, Switzerland
[3] Univ Alberta, Dept Chem, Edmonton, AB, Canada
[4] Univ Nacl Autonoma Mexico, Mexico City, DF, Mexico
[5] Janelia Res Campus, Howard Hughes Med Inst, GENIE Project, Ashburn, VA USA
[6] Boston Univ, Dept Biol, 5 Cummington St, Boston, MA 02215 USA
[7] Stanford Univ, Dept Biol, Stanford, CA 94305 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
MICROSCOPY; PATHWAYS; PROTEIN;
D O I
10.1038/s41592-020-0835-7
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
jYCaMP1, a yellow variant of the calcium indicator jGCaMP7, enables fast multicolor two-photon imaging at excitation wavelengths above 1,000 nm for use with popular ytterbium-doped fiber and modelocked semiconductor lasers. Femtosecond lasers at fixed wavelengths above 1,000 nm are powerful, stable and inexpensive, making them promising sources for two-photon microscopy. Biosensors optimized for these wavelengths are needed for both next-generation microscopes and affordable turn-key systems. Here we report jYCaMP1, a yellow variant of the calcium indicator jGCaMP7 that outperforms its parent in mice and flies at excitation wavelengths above 1,000 nm and enables improved two-color calcium imaging with red fluorescent protein-based indicators.
引用
收藏
页码:694 / +
页数:7
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