Abstract
Chloride (Cl-) channels are membrane proteins that consist of Cl- permeation pores capable of transporting Cl- ions across lipid membranes. In doing so, they play many important roles in maintaining the physiological functions of various cells, and malfunction of these membrane proteins leads to a variety of hereditary diseases, such as epilepsy, myotonia, and cystic fibrosis. Various types of Cl- channels have been identified with different structures and functions. This chapter discusses the structures and mechanisms of two specific types of Cl- channels - CLC Cl- channels and CFTR Cl- channels. Because homologous molecules of these two types of Cl- channels can function as transporters, the transporter mechanisms related to the functions of Cl- channels are also discussed.
Original language | English |
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Title of host publication | Comprehensive Biophysics |
Publisher | Elsevier Inc. |
Pages | 142-176 |
Number of pages | 35 |
Volume | 6 |
ISBN (Print) | 9780080957180 |
DOIs | |
State | Published - 2012 |
Keywords
- ABC transporters
- ATP
- CFTR
- CLC family
- Gating
- Membrane transport
- Permeation
- Phosphorylation
- Structure and function
- Voltage dependence