Liquid–liquid phase separation facilitates the biogenesis of secretory storage granules

Author:

Parchure Anup1ORCID,Tian Meng1ORCID,Stalder Danièle2ORCID,Boyer Cierra K.34ORCID,Bearrows Shelby C.34ORCID,Rohli Kristen E.34ORCID,Zhang Jianchao56ORCID,Rivera-Molina Felix1,Ramazanov Bulat R.1ORCID,Mahata Sushil K.78,Wang Yanzhuang56ORCID,Stephens Samuel B.3,Gershlick David C.2ORCID,von Blume Julia1ORCID

Affiliation:

1. Department of Cell Biology, Yale University School of Medicine, New Haven, CT 1

2. Cambridge Institute for Medical Research, University of Cambridge, Cambridge, UK 2

3. Departments of Pharmacology and Neuroscience, Fraternal Order of Eagles Diabetes Research Center, University of Iowa, Iowa City, IA 3

4. Internal Medicine, Division of Endocrinology and Metabolism, University of Iowa, Iowa City, IA 4

5. Department of Molecular, Cellular and Developmental Biology, University of Michigan, Ann Arbor, MI 5

6. Department of Neurology, University of Michigan School of Medicine, Ann Arbor, MI 6

7. Department of Medicine, University of California San Diego, La Jolla, CA 7

8. VA San Diego Healthcare System, San Diego, CA 8

Abstract

Insulin is synthesized by pancreatic β-cells and stored into secretory granules (SGs). SGs fuse with the plasma membrane in response to a stimulus and deliver insulin to the bloodstream. The mechanism of how proinsulin and its processing enzymes are sorted and targeted from the trans-Golgi network (TGN) to SGs remains mysterious. No cargo receptor for proinsulin has been identified. Here, we show that chromogranin (CG) proteins undergo liquid–liquid phase separation (LLPS) at a mildly acidic pH in the lumen of the TGN, and recruit clients like proinsulin to the condensates. Client selectivity is sequence-independent but based on the concentration of the client molecules in the TGN. We propose that the TGN provides the milieu for converting CGs into a “cargo sponge” leading to partitioning of client molecules, thus facilitating receptor-independent client sorting. These findings provide a new receptor-independent sorting model in β-cells and many other cell types and therefore represent an innovation in the field of membrane trafficking.

Publisher

Rockefeller University Press

Subject

Cell Biology

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