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bioRxiv · 10.1101/2020.01.17.910125

Retromer retrieves the Wilson Disease protein, ATP7B from lysosomes in a copper-dependent mode

Gupta, A.·Das, S.·Maji, S.·NA, R.·Saha, T.·Bhattacharya, I.
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Abstract

ATP7B utilizes lysosomal exocytosis to export copper from hepatocytes. We investigated the fate of ATP7B, post-copper export. At high copper ATP7B traffics to lysosomes and upon subsequent copper chelation, returns to Trans Golgi Network. At high copper, ATP7B co-localizes with lysosomal marker, Lamp1 and the core member of retromer complex, Vps35. Knocking down VPS35 did not alter copper-responsive vesicularization of ATP7B; rather upon subsequent copper chelation, ATP7B failed to relocalize to TGN that could be rescued by overexpressing wtVPS35. Using super-resolution microscopy and proximity ligation assays we demonstrate that VPS35 and ATP7B are juxtaposed on the same lysosomal compartment and their interaction is indirect. Utilizing in-cell photoamino acid-based UV-crosslinking and subsequent immunoprecipitation, we detected ATP7B and retromer subunits, VPS35 and VPS26 in a large complex in high copper conditions, hence confirming their interaction. We demonstrate that retromer regulates lysosome to TGN trafficking of the copper transporter ATP7B and it is dependent upon cellular copper level.

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Gupta, A., Das, S., Maji, S., NA, R., Saha, T., Bhattacharya, I.. 2020-01-17. Retromer retrieves the Wilson Disease protein, ATP7B from lysosomes in a copper-dependent mode. https://doi.org/10.1101/2020.01.17.910125

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