费斯特共振能量转移
拟南芥
生物
胞浆
生物物理学
拟南芥
细胞生物学
双分子荧光互补
蛋白激酶结构域
钙信号传导
生物化学
化学
信号转导
荧光
突变体
酶
物理
基因
量子力学
酵母
作者
Anja Liese,Bernadette Eichstädt,Sarah Lederer,Philipp Schulz,Jan Oehlschläger,Susanne Matschi,José A. Feijó,Waltraud X. Schulze,Kai R. Konrad,Tina Romeis
出处
期刊:The Plant Cell
[Oxford University Press]
日期:2023-07-11
卷期号:36 (2): 276-297
被引量:7
标识
DOI:10.1093/plcell/koad196
摘要
Changes in cytosolic calcium (Ca2+) concentration are among the earliest reactions to a multitude of stress cues. While a plethora of Ca2+-permeable channels may generate distinct Ca2+ signatures and contribute to response specificities, the mechanisms by which Ca2+ signatures are decoded are poorly understood. Here, we developed a genetically encoded Förster resonance energy transfer (FRET)-based reporter that visualizes the conformational changes in Ca2+-dependent protein kinases (CDPKs/CPKs). We focused on two CDPKs with distinct Ca2+-sensitivities, highly Ca2+-sensitive Arabidopsis (Arabidopsis thaliana) AtCPK21 and rather Ca2+-insensitive AtCPK23, to report conformational changes accompanying kinase activation. In tobacco (Nicotiana tabacum) pollen tubes, which naturally display coordinated spatial and temporal Ca2+ fluctuations, CPK21-FRET, but not CPK23-FRET, reported oscillatory emission ratio changes mirroring cytosolic Ca2+ changes, pointing to the isoform-specific Ca2+-sensitivity and reversibility of the conformational change. In Arabidopsis guard cells, CPK21-FRET-monitored conformational dynamics suggest that CPK21 serves as a decoder of signal-specific Ca2+ signatures in response to abscisic acid and the flagellin peptide flg22. Based on these data, CDPK-FRET is a powerful approach for tackling real-time live-cell Ca2+ decoding in a multitude of plant developmental and stress responses.
科研通智能强力驱动
Strongly Powered by AbleSci AI