Brumbaugh Justin, Schleifenbaum Andreas, Gasch Alexander, Sattler Michael, Schultz Carsten
European Molecular Biology Institute (EMBL), Meyerhofstrasse 1, 69117 Heidelberg, Germany.
J Am Chem Soc. 2006 Jan 11;128(1):24-5. doi: 10.1021/ja0562200.
Cell function is regulated by complex and often interdependent networks of signaling molecules. To accurately describe these networks, it is important to monitor multiple signals in parallel. To this end, we have developed a genetically encoded, FRET-based probe that independently monitors both protein kinase A (PKA) and protein kinase C (PKC) activity in vivo. Artificial as well as physiological stimulants produced a negative or positive change in FRET efficiency following PKA or PKC activation, respectively. Mutations of the phosphate-accepting amino acids of the PKC substrate yielded a probe that was sensitive to PKA activation alone.
细胞功能由复杂且通常相互依存的信号分子网络调控。为准确描述这些网络,并行监测多种信号很重要。为此,我们开发了一种基于荧光共振能量转移(FRET)的基因编码探针,可在体内独立监测蛋白激酶A(PKA)和蛋白激酶C(PKC)的活性。人工刺激剂和生理刺激剂分别在PKA或PKC激活后使FRET效率产生负向或正向变化。PKC底物的磷酸化接受氨基酸发生突变后产生了一种仅对PKA激活敏感的探针。