Sorting Nexins in Protein Homeostasis

• Published in: Cells (Basel, Switzerland) Vol. 10; no. 1; p. 17
• Main Authors: Hanley, Sara E, Cooper, Katrina F
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 24.12.2020; MDPI
• Subjects: Autophagy; Binding sites; Cardiovascular diseases; Cell adhesion & migration; Cell cycle; Disease; endosome; Homeostasis; Human papillomavirus; lysosome; Mammals; Membranes; Mutation; Organelles; Phagocytosis; Plasma; Proteasomes; Protein folding; Protein transport; Proteins; Quality control; Recycling; retromer; Review; Severe acute respiratory syndrome coronavirus 2; Signal transduction; sorting nexins; Ubiquitin; proteasome; endosome; autophagy; retromer; sorting nexins; lysosome; ubiquitin
• ISSN: 2073-4409; 2073-4409
• DOI: 10.3390/cells10010017

Protein homeostasis is maintained by removing misfolded, damaged, or excess proteins and damaged organelles from the cell by three major pathways; the ubiquitin-proteasome system, the autophagy-lysosomal pathway, and the endo-lysosomal pathway. The requirement for ubiquitin provides a link between all three pathways. Sorting nexins are a highly conserved and diverse family of membrane-associated proteins that not only traffic proteins throughout the cells but also provide a second common thread between protein homeostasis pathways. In this review, we will discuss the connections between sorting nexins, ubiquitin, and the interconnected roles they play in maintaining protein quality control mechanisms. Underlying their importance, genetic defects in sorting nexins are linked with a variety of human diseases including neurodegenerative, cardiovascular diseases, viral infections, and cancer. This serves to emphasize the critical roles sorting nexins play in many aspects of cellular function.