Closed ValWood closed 1 year ago
New Nature paper reconstituting membrane curvature with purified components:
Nature. 2017 Feb 22. doi: 10.1038/nature21387. [Epub ahead of print] Reconstitution of the tubular endoplasmic reticulum network with purified components. Powers RE1,2, Wang S1,2, Liu TY1,2, Rapoport TA1,2. Author information Abstract Organelles display characteristic morphologies that are intimately tied to their cellular function, but how organelles are shaped is poorly understood. The endoplasmic reticulum is particularly intriguing, as it comprises morphologically distinct domains, including a dynamic network of interconnected membrane tubules. Several membrane proteins have been implicated in network formation, but how exactly they mediate network formation and whether they are all required are unclear. Here we reconstitute a dynamic tubular membrane network with purified endoplasmic reticulum proteins. Proteoliposomes containing the membrane-fusing GTPase Sey1p (refs 6, 7) and the curvature-stabilizing protein Yop1p (refs 8, 9) from Saccharomyces cerevisiae form a tubular network upon addition of GTP. The tubules rapidly fragment when GTP hydrolysis of Sey1p is inhibited, indicating that network maintenance requires continuous membrane fusion and that Yop1p favours the generation of highly curved membrane structures. Sey1p also forms networks with other curvature-stabilizing proteins, including reticulon and receptor expression-enhancing proteins (REEPs) from different species. Atlastin, the vertebrate orthologue of Sey1p, forms a GTP-hydrolysis-dependent network on its own, serving as both a fusion and curvature-stabilizing protein. Our results show that organelle shape can be generated by a surprisingly small set of proteins and represents an energy-dependent steady state between formation and disassembly.
The MICOS component Mic60 displays a conserved membrane-bending activity that is necessary for normal cristae morphology. J Cell Biol. 2017 Mar 2;. [Epub ahead of print] PMID: 28254827
See also this comment in older closed ticket: geneontology/go-ontology#12387
I wonder if "membrane bending" should be a Molecular function, rather than a biological process? https://en.wikipedia.org/wiki/Membrane_curvature#Proteins_can_Induce_Curvature
@ukemi @thomaspd
It feels like a function
Can I add a vote for membrane bending being an MF - this is the activity of BAR domain proteins.
PMID:27720484, EndoA: "Helix H1 inserts deep into the lipid bilayer, causing shallow membrane curvature and the formation of tubules on in vitro membranes. By contrast, when EndoA is phosphorylated, the protein inserts less deeply into the lipid bilayer, causing increased curvature by wedging Helix H1 into the lipid head group region"
@pgaudet - This ticket seems overlapping with a new one @ValWood just made that is assigned to me (#14593). For efficiency, I think it would be better if one of us did both of these. I have a long standing interest in this since trying to get a MF term to annotate a yeast protein in SGD, so I'd be happy to take this one too.
reassigned, thanks for pointing it out.
Pascale
https://github.com/geneontology/go-ontology/issues/12387
There still seem to be some connections missing: