荧光
巴普塔
化学
生物物理学
生物化学
光学成像
荧光蛋白
计算生物学
纳米技术
荧光寿命成像显微镜
集合(抽象数据类型)
计算机科学
选择性
光学(聚焦)
绿色荧光蛋白
作者
Xinqi Zhou,Kayla J. Belavek,Evan W. Miller
出处
期刊:Biochemistry
[American Chemical Society]
日期:2021-07-12
卷期号:60 (46): 3547-3554
被引量:32
标识
DOI:10.1021/acs.biochem.1c00350
摘要
In 1980, Roger Tsien published a paper, in this journal [Tsien, R. Y. (1980) Biochemistry, 19 (11), 2396], titled "New calcium indicators and buffers with high selectivity against magnesium and protons: design, synthesis, and properties of prototype structures". These new buffers included 1,2-bis(o-aminophenoxy)ethane-N,N,N',N'-tetraacetic acid, or BAPTA, which is still widely used today. And so, the world was set alight with new ways in which to visualize Ca2+. The ability to watch fluctuations in intracellular Ca2+ revolutionized the life sciences, although the fluorescent indicators used today, particularly in neurobiology, no longer rely exclusively on BAPTA but on genetically encoded fluorescent Ca2+ indicators. In this Perspective, we reflect on the origins of Ca2+ imaging with a special focus on the contributions made by Roger Tsien, from the early concept of selective Ca2+ binding described in Biochemistry to optical Ca2+ indicators based on chemically synthesized fluorophores to genetically encoded fluorescent Ca2+ indicators.
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