Investigating signal transduction with genetically encoded fluorescent probes - Delivered on 22 October 2002 at the 28th FEBS Meeting in Istanbul

被引:13
作者
Pozzan, T
Mongillo, M
Rudolf, R
机构
[1] Univ Padua, Dept Biomed Sci, CNR, Inst Neurosci, I-35121 Padua, Italy
[2] Venetian Inst Mol Med, Padua, Italy
来源
EUROPEAN JOURNAL OF BIOCHEMISTRY | 2003年 / 270卷 / 11期
关键词
D O I
10.1046/j.1432-1033.2003.03615.x
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
Ca2+ and cAMP are ubiquitous second messengers in eukaryotes and control numerous physiological responses ranging from fertilization to cell death induction. To distinguish between these different responses, their subtle regulation in time, space and amplitude is needed. Therefore, the characterization of the signalling process requires measurement of second messengers with tools of precise localization, high dynamic range and as little disturbance of cell physiology as possible. Recently, fluorescent proteins of marine jellyfish have given rise to a set of genetically encoded biosensors which fulfil these criteria and which have already led to important new insights into the subcellular handling of Ca2+ and cAMP. The use of these probes in combination with new microscopical methods such as two-photon microscopy now enables researchers to study second messenger signalling in intact tissues. In this review, the genetically encoded measurement probes and their origin are briefly introduced and some recent insights into the spatio-temporal complexity of both Ca2+ and cAMP signalling obtained with these tools are discussed.
引用
收藏
页码:2343 / 2352
页数:10
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