During the last decade it has become evident that autophagy is not simply a non-selective bulk degradation pathway for intracellular components. On the contrary, the discovery and characterization of autophagy receptors which target specific cargo for lysosomal degradation by interaction with ATG8 (autophagy-related protein 8)/LC3 (light-chain 3) has accelerated our understanding of selective autophagy. A number of autophagy receptors have been identified which specifically mediate the selective autophagosomal degradation of a variety of cargoes including protein aggregates, signalling complexes, midbody rings, mitochondria and bacterial pathogens. In the present chapter, we discuss these autophagy receptors, their binding to ATG8/LC3 proteins and how they act in ubiquitin-mediated selective autophagy of intracellular bacteria (xenophagy) and protein aggregates (aggrephagy).
Skip Nav Destination
Article navigation
September 2013
Issue Editors
-
Cover Image
Cover Image
- PDF Icon PDF LinkFront Matter
Review Article|
September 27 2013
Selective autophagy
Steingrim Svenning;
Steingrim Svenning
Molecular Cancer Research Group, Institute of Medical Biology, University of Tromsø, 9037 Tromsø, Norway
Search for other works by this author on:
Terje Johansen
Terje Johansen
1
Molecular Cancer Research Group, Institute of Medical Biology, University of Tromsø, 9037 Tromsø, Norway
1To whom correspondence should be addressed (email [email protected]).
Search for other works by this author on:
Publisher: Portland Press Ltd
Online ISSN: 1744-1358
Print ISSN: 0071-1365
© The Authors Journal compilation © 2013 Biochemical Society
2013
Essays Biochem (2013) 55: 79–92.
Citation
Jon D. Lane, Steingrim Svenning, Terje Johansen; Selective autophagy. Essays Biochem 27 September 2013; 55 79–92. doi: https://doi.org/10.1042/bse0550079
Download citation file:
Sign in
Don't already have an account? Register
Sign in to your personal account
You could not be signed in. Please check your email address / username and password and try again.
Could not validate captcha. Please try again.