Structure of the Human Signal Peptidase Complex Reveals the Determinants for Signal Peptide Cleavage

Abstract

The signal peptidase complex (SPC) is an essential membrane complex in the endoplasmic reticulum (ER), here it removes signal peptides (SPs) from a large variety of secretory pre-proteins with exquisite specificity. Although the determinants of this process have been established empirically, the molecular details of SP recognition and removal remain elusive. Here, we show that the human SPC exists in two functional paralogs with distinct roteolytic subunits. We determined the atomic structures of both paralogs using electron cryo-microscopy and tructural proteomics. The active site is formed by a catalytic triad and abuts the ER membrane, where a transmembrane window collectively formed by all subunits locally thins the bilayer. This unique architecture generates specificity for thousands of SPs based on the length of their hydrophobic segments.