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VPS13B is localized at the interface between Golgi cisternae and is a functional partner of FAM177A1

6 Aug 2024

Abstract excerpt

Mutations in VPS13B, a member of a protein family implicated in bulk lipid transport between adjacent membranes, cause Cohen syndrome. VPS13B is known to be concentrated in the Golgi complex, but its precise location within this organelle and thus the site(s) where it achieves lipid transport remains unclear. Here, we show that VPS13B is localized at the interface between proximal and distal Golgi subcompartments...

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Share to Cellular transport and secretion
Share to Erythrocyte Function and Pathophysiology
Share to Lipid Membrane Structure and Behavior

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PMID: 39331042
DOI: 10.1083/jcb.202311189

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026.

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