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• W2593854881 abstract "Significance Cystic fibrosis is caused by mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene that encodes a chloride channel located in the apical membrane of epithelia cells. The cAMP signaling pathway and protein phosphorylation are known to be primary controlling mechanisms for channel function. In this study, we present an alternative activation pathway that involves calcium-activated calmodulin binding of the intrinsically disordered regulatory (R) region of CFTR. Beyond their potential therapeutic value, these data provide insights into the intersection of calcium signaling with control of ion homeostasis and the ways in which the local CFTR microdomain organizes itself." @default.
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• W2593854881 date "2017-02-27" @default.
• W2593854881 modified "2023-10-14" @default.
• W2593854881 title "Synergy of cAMP and calcium signaling pathways in CFTR regulation" @default.
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• W2593854881 doi "https://doi.org/10.1073/pnas.1613546114" @default.
• W2593854881 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/5358358" @default.
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