Abstract
Autophagy is an important lysosomal degradation pathway that aids in the maintenance of cellular homeostasis by breaking down and recycling intracellular contents. Dysregulation of autophagy is linked to a growing number of human diseases. The Beclin 1-Vps34 protein-protein interaction network is critical for autophagy regulation and is therefore essential to cellular integrity. Manipulation of autophagy, in particular via modulation of the action of the Beclin 1-Vps34 complexes, is considered a promising route to combat autophagy-related diseases. Here we summarize recent findings on the core components and structural architecture of the Beclin 1-Vps34 complexes, and how these findings provide valuable insights into the molecular mechanisms that underlie the multiple functions of these complexes and for devising therapeutic strategies.
Original language | English |
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Pages (from-to) | 398-426 |
Number of pages | 29 |
Journal | Frontiers in Biology |
Volume | 10 |
Issue number | 5 |
DOIs | |
State | Published - Oct 1 2015 |
Bibliographical note
Publisher Copyright:© 2015, Higher Education Press and Springer-Verlag Berlin Heidelberg.
Keywords
- Beclin 1
- CX-MS
- EM
- Nrbf2
- Vps34
- complex
- drug design
- inhibitor
- structure
ASJC Scopus subject areas
- Biotechnology
- Ecology, Evolution, Behavior and Systematics
- Ecology
- Genetics