Literature DB >> 33169667

A physical mechanism of TANGO1-mediated bulky cargo export.

Ishier Raote1, Morgan Chabanon2,3, Nikhil Walani3, Marino Arroyo3,4,5, Maria F Garcia-Parajo2,6, Vivek Malhotra1,6,7, Felix Campelo2.   

Abstract

The endoplasmic reticulum (ER)-resident protein TANGO1 assembles into a ring around ER exit sites (ERES), and links procollagens in the ER lumen to COPII machinery, tethers, and ER-Golgi intermediate compartment (ERGIC) in the cytoplasm (Raote et al., 2018). Here, we present a theoretical approach to investigate the physical mechanisms of TANGO1 ring assembly and how COPII polymerization, membrane tension, and force facilitate the formation of a transport intermediate for procollagen export. Our results indicate that a TANGO1 ring, by acting as a linactant, stabilizes the open neck of a nascent COPII bud. Elongation of such a bud into a transport intermediate commensurate with bulky procollagens is then facilitated by two complementary mechanisms: (i) by relieving membrane tension, possibly by TANGO1-mediated fusion of retrograde ERGIC membranes and (ii) by force application. Altogether, our theoretical approach identifies key biophysical events in TANGO1-driven procollagen export.
© 2020, Raote et al.

Entities:  

Keywords:  budding; cell biology; membrane curvature; membrane dynamics; membrane tension; none; physics of living systems; procollagen export; secretory pathway

Year:  2020        PMID: 33169667      PMCID: PMC7704110          DOI: 10.7554/eLife.59426

Source DB:  PubMed          Journal:  Elife        ISSN: 2050-084X            Impact factor:   8.140


  84 in total

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