NEDD4-2 (NEDD4L): the ubiquitin ligase for multiple membrane proteins

P Goel, JA Manning, S Kumar - Gene, 2015 - Elsevier
Abstract NEDD4-2 (also known as NEDD4L, neural precursor cell expressed
developmentally down-regulated 4-like) is a ubiquitin protein ligase of the Nedd4 family …

From the endoplasmic reticulum to the plasma membrane: mechanisms of CFTR folding and trafficking

CM Farinha, S Canato - Cellular and Molecular Life Sciences, 2017 - Springer
CFTR biogenesis starts with its co-translational insertion into the membrane of endoplasmic
reticulum and folding of the cytosolic domains, towards the acquisition of a fully folded …

Endocytosis: a turnover mechanism controlling ion channel function

I Estadella, O Pedrós-Gámez, M Colomer-Molera… - Cells, 2020 - mdpi.com
Ion channels (IChs) are transmembrane proteins that selectively drive ions across
membranes. The function of IChs partially relies on their abundance and proper location in …

Influenza virus infection alters ion channel function of airway and alveolar cells: mechanisms and physiological sequelae

JD Londino, A Lazrak, JF Collawn… - … of Physiology-Lung …, 2017 - journals.physiology.org
The cystic fibrosis transmembrane conductance regulator (CFTR) and the amiloride-
sensitive epithelial sodium channels (ENaC) are located in the apical membranes of airway …

The cellular pathways that maintain the quality control and transport of diverse potassium channels

NH Nguyen, JL Brodsky - Biochimica et Biophysica Acta (BBA)-Gene …, 2023 - Elsevier
Potassium channels are multi-subunit transmembrane proteins that permit the selective
passage of potassium and play fundamental roles in physiological processes, such as …

Peripheral protein quality control as a novel drug target for CFTR stabilizer

R Fukuda, T Okiyoneda - Frontiers in Pharmacology, 2018 - frontiersin.org
Conformationally defective cystic fibrosis transmembrane conductance regulator (CFTR)
including rescued ΔF508-CFTR is rapidly eliminated from the plasma membrane (PM) even …

Biosynthesis of cystic fibrosis transmembrane conductance regulator

IM Pranke, I Sermet-Gaudelus - The international journal of biochemistry & …, 2014 - Elsevier
The cystic fibrosis transmembrane conductance regulator (CFTR) is a cAMP-regulated
chloride (Cl−) channel. Mutations of its gene lead to the disease of cystis fibrosis (CF) …

[HTML][HTML] An outlined review for the role of Nedd4-1 and Nedd4-2 in lung disorders

H He, C Huang, Z Chen, H Huang, X Wang… - Biomedicine & …, 2020 - Elsevier
Neural precursor cell expressed, developmentally down-regulated 4, E3 ubiquitin protein
ligase (Nedd4-1 and Nedd4-2) is a member of the HECT E3 ubiquitin ligase family. It has …

ΔF508 CFTR surface stability is regulated by DAB2 and CHIP-mediated ubiquitination in post-endocytic compartments

L Fu, A Rab, L Tang, Z Bebok, SM Rowe… - PLoS …, 2015 - journals.plos.org
The ΔF508 mutant form of the cystic fibrosis transmembrane conductance regulator (ΔF508
CFTR) that is normally degraded by the ER-associated degradative pathway can be rescued …

Chapter five-ubiquitination of ion channels and transporters

SM Lamothe, S Zhang - Progress in molecular biology and translational …, 2016 - Elsevier
Ion channels and transporters play essential roles in excitable cells including cardiac,
skeletal, and smooth muscle cells, neurons, and endocrine cells. Their dysfunction underlies …