Article

VPS13B is localized at the cis-trans Golgi complex interface and is a functional partner of FAM177A1

2023-12-18

Abstract excerpt

<h4>ABSTRACT</h4> 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 cis and trans Golgi sub-...

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Literature Corpus work: bfa5a0b4-90ee-559b-8eff-4b34b0ce885e
DOI: 10.1101/2023.12.18.572081

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