Components and Mechanisms of Import, Modification, Folding, and Assembly of Immunoglobulins in the Endoplasmic Reticulum

Abstract

In mammalian cells, the endoplasmic reticulum (ER) plays a central role in biogenesis of secretory- and plasma membrane proteins as well as in cellular calcium (Ca(2+)) homeostasis. The protein biogenesis function involves an aqueous polypeptide conducting channel in the ER membrane, which is formed by the heterotrimeric Sec61 complex; the store- and receptor-controlled Ca(2+)- release function requires a steep ER to cytosol gradient, with more than 500μM free Ca(2+) in the ER and 50nM Ca(2+) in the cytosol. Recent work demonstrated that the Sec61 complex can transiently allow passive ER Ca(2+) efflux. Therefore, gating of the Sec61 channel has to be tightly regulated by substrates as well as allosteric effectors. The ER lumenal Hsp70-type molecular chaperone, immunoglobulin heavy-chain binding protein (BiP), together with its membrane resident co-chaperone Sec63 facilitates channel opening in a precursor specific manner. In addition, BiP, together with its lumenal co-chaperones, ERj3 and ERj6, as well as cytosolic Ca(2+)-calmodulin (CaM) in collaboration with the membrane resident Sec62 protein represent allosteric effectors for channel closure. In the course of the last couple of years several human diseases were linked to the Sec61 complex and its effectors and were termed Sec61-channelopathies.