Final answer:
The cystic fibrosis transmembrane regulator (CFTR) is an ABC transporter that functions as a Cl⁻ ion channel in both healthy individuals and individuals with cystic fibrosis (CF).
Step-by-step explanation:
The cystic fibrosis transmembrane regulator (CFTR) is an ABC transporter that functions as a Cl⁻ ion channel.
In healthy people, the CFTR protein transports Cl- ions out of the cell. However, in individuals with cystic fibrosis (CF), the mutated CFTR gene produces a defective channel protein that is not incorporated into the membrane.
The CFTR requires ATP to function, allowing the transport of Cl- ions out of the cell. This form of transport is considered active transport, as the Cl- ions are flowing down their concentration gradient.