Key result
A kinase anchoring proteins (AKAPs) play an emerging role in regulating the three main cardiac phosphatases: Protein Phosphatase 1, 2A, and 2B.
AKAPs play a critical role in the heart by acting as molecular scaffolds that coordinate the activity of key cardiac phosphatases.
AKAP-phosphatase interactions remain preclinical; leaves open targeted modulation as a therapeutic strategy in heart disease.
Directed protein phosphorylation is indisputably critical for a multitude of cellular processes. A growing body of research demonstrates A kinase anchoring proteins (AKAPs) to mediate a significant number of phosphorylation events in the heart. By acting as molecular tethers for the regulatory subunit of protein kinase A, AKAPs focus kinase activity onto specific substrate. In the time since their discovery, the AKAP model has evolved in appreciation of the broader role these scaffolds play in coordinating multiple signaling enzymes to efficiently regulate dynamic cellular processes. The focus of this review is on the emerging role of AKAPs in regulating the 3 main cardiac phosphatases: Protein Phosphatase 1 by AKAP18 and Yotiao, and Protein Phosphatases 2A and 2B by muscle specific A-kinase anchoring protein.
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Redden et al. (2011) conducted a review in Cardiac phosphatase regulation. A kinase anchoring proteins (AKAPs) was evaluated. A kinase anchoring proteins (AKAPs) play an emerging role in regulating the three main cardiac phosphatases: Protein Phosphatase 1, 2A, and 2B.
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