A hollow TFG condensate spatially compartmentalizes the early secretory pathway
In the early secretory pathway, endoplasmic reticulum (ER) and Golgi membranes form a nearly spherical interface. In this ribosome-excluding zone, bidirectional transport of cargo coincides with a spatial segregation of anterograde and retrograde carriers by an unknown mechanism. We show that at physiological conditions, the Trk-fused gene (TFG) self-organizes to form a hollow, anisotropic condensate that matches the dimensions of the ER-Golgi interface and is dynamically regulated across the cell cycle. Regularly spaced hydrophobic residues in TFG control the condensation mechanism and result in a porous condensate surface. We find that TFG condensates act as a molecular sieve capable of allowing access of anterograde coats (COPII) to the condensate interior while restricting retrograde coats (COPI). We propose that a hollow TFG condensate structures the ER-Golgi interface to create a diffusion-limited space for anterograde transport. We further propose that TFG condensates optimize membrane flux by insulating secretory carriers in their lumen from retrograde carriers outside TFG cages.
Authors
- Ingrid R. Niesman (ORCID: https://orcid.org/0000-0001-9767-6629)
- Andreas M. Ernst
- Miguel Ruiz
- Sharon W. Y. Cheung
- William R. Wegeng
- Savannah M Bogus (ORCID: https://orcid.org/0009-0008-3355-2203)
- Khalid S. M. Noori
- Sindy R. Chavez
Institutions
- San Diego State University (US)
- University of California San Diego (US)
Publication Details
- Journal
- Nature Communications
- Published
- 2025-04-19
- DOI
- https://doi.org/10.1038/s41467-025-59118-1
- Citations
- 5
- Primary Topic
- Cellular transport and secretion
- Type
- article
- Field-Weighted Citation Impact
- 5.76
Funders
- Directorate for Biological Sciences
- University of California, San Diego
- National Institute of General Medical Sciences
- National Institute of Neurological Disorders and Stroke