Article
Protein interactions, calcium, phosphorylation, and cholesterol modulate CFTR cluster formation on membranes
2024-05-06
Abstract excerpt
<h4>ABSTRACT</h4> The Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) is a chloride channel whose dysfunction leads to intracellular accumulation of chloride ions, dehydration of cell surfaces, and subsequent damage to airway and ductal organs. Beyond its function as a chloride channel, interactions between CFTR, ENaC, and SLC transporter family membrane proteins and cytoplasmic proteins, including cal...
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Identifiers and source
- Literature Corpus work
- 31b65067-5c41-562e-b2eb-96161414a461
- DOI
- 10.1101/2024.05.03.592454
