COPII-coated membranes function as transport carriers of intracellular procollagen I

Abstract

The coat protein complex II (COPII) is essential for the secretion of large cargo, such as procollagen I (PC1), but evidence that COPII vesicles act as PC1 transport carriers from the ER was lacking. Using high-resolution microscopy and in vitro reconstituted vesicle budding assays, Gorur et al. show that COPII vesicles carry PC1.

Abstract

The coat protein complex II (COPII) is essential for the transport of large cargo, such as 300-nm procollagen I (PC1) molecules, from the endoplasmic reticulum (ER) to the Golgi. Previous work has shown that the CUL3-KLHL12 complex increases the size of COPII vesicles at ER exit sites to more than 300 nm in diameter and accelerates the secretion of PC1. However, the role of large COPII vesicles as PC1 transport carriers was not unambiguously demonstrated. In this study, using stochastic optical reconstruction microscopy, correlated light electron microscopy, and live-cell imaging, we demonstrate the existence of mobile COPII-coated vesicles that completely encapsulate the cargo PC1 and are physically separated from ER. We also developed a cell-free COPII vesicle budding reaction that reconstitutes the capture of PC1 into large COPII vesicles. This process requires COPII proteins and the GTPase activity of the COPII subunit SAR1. We conclude that large COPII vesicles are bona fide carriers of PC1.