Membrane curvature sensing and stabilization by the autophagic LC3 lipidation machinery
Open accessPreprint — published as 10.1126/sciadv.add1436
Abstract
How the highly curved phagophore membrane is stabilized during autophagy initiation is a major open question in autophagosome biogenesis. Here, we use in vitro reconstitution on membrane nanotubes and molecular dynamics simulations to investigate how core autophagy proteins in the LC3 lipidation cascade interact with curved membranes, providing insight into possible roles in regulating membrane shape during autophagosome biogenesis. ATG12–5-16L1 was up to 100-fold enriched on highly curved nanotubes relative to flat membranes. At high surface density, ATG12–5-16L1 binding increased the curvature of the nanotubes. While WIPI2 binding directs membrane recruitment, the amphipathic helix α 2 of ATG16L1 is responsible for curvature sensitivity. Molecular dynamics simulations revealed that helix α 2 of ATG16L1 inserts shallowly into the membrane, explaining its curvature-sensitive binding to the membrane. These observations show how the binding of the ATG12–5-16L1 complex to the early phagophore rim could stabilize membrane curvature and facilitate autophagosome growth.
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Highly accurate protein structure prediction with AlphaFold
Jumper, J., Evans, R., Pritzel, A., Green, T., Figurnov, M., Ronneberger, O., Tunyasuvunakool, K., Bates, R., Žídek, A., Potapenko, A., et al. (2021) · Nature · doi:10.1038/s41586-021-03819-2 · Cited by 43,764 · see citing works
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Mesoscale simulation of biomembranes with FreeDTS
Pezeshkian, W., & Ipsen, J. H. (2024) · Nature Communications · doi:10.1038/s41467-024-44819-w · Cited by 24 · see citing works
“Examples of exciting developments include the local curvature of membranes caused by a single protein or by the assembly of proteins [12-14], membrane shape induced lipid sorting[15], wetting induced membrane deformation [16], and even curvature sensing of proteins[17].”
- Authors
- Jensen, L. E., Rao, S., Schuschnig, M., Cada, A. K., Martens, S., Hummer, G., & Hurley, J. H.
- Affiliations
- QB3 (US)
- Max Planck Institute of Biophysics (DE)
- University of Vienna (AT)
- Goethe University Frankfurt (DE)
- Corresponding author
- Hurley, James H.
- ORCID
- Venue
- Science Advances
- Publisher
- openRxiv
- Published
- 2022-05-04
- Volume
- 8
- Issue
- 50
- Pages
- eadd1436-eadd1436
- ISSN
- 2375-2548 (ISSN-L)
- PMC
- PMC9750143
- OpenAlex
- W4311441084
- Cited by
- 49
- References
- 1
- Citations by year
- 2026: 8 · 2025: 9 · 2024: 12 · 2023: 19 · 2022: 1
- FWCI
- 7.40
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- cc-by
- Locations
- Science Advances (publishedVersion, cc-by)
- bioRxiv (Cold Spring Harbor Laboratory) (acceptedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- eScholarship (California Digital Library) (submittedVersion, cc-by)
- Funders
- Michael J. Fox Foundation for Parkinson's Research (ASAP-000350)
- Max-Planck-Gesellschaft
- National Institutes of Health
- National Institute of General Medical Sciences (GM111730, R01GM111730)
- National Institute of Allergy and Infectious Diseases (F31AI150312)
- Topics
- Health Sciences › Medicine › Epidemiology › Autophagy in Disease and Therapy
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Cellular transport and secretion
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Lipid Membrane Structure and Behavior
- Keywords
- autophagy, autophagosome formation, membrane curvature, LC3 lipidation, WIPI2, phagophore, tunneling nanotubes, membrane curvature sensing, protein-membrane binding
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