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Signal peptide peptidase (SPP) catalyzes intramembrane proteolysis of some signal peptides after they have been cleaved from a preprotein. In humans, SPP activity is required to generate signal sequence-derived human lymphocyte antigen-E epitopes that are recognized by the immune system, and to process hepatitis C virus core protein. We have identified human SPP as a polytopic membrane protein with sequence motifs characteristic of the presenilin-type aspartic proteases. SPP and potential eukaryotic homologs may represent another family of aspartic proteases that promote intramembrane proteolysis to release biologically important peptides.
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Andreas Weihofen
Biogen (United States)
Kathleen L. Binns
Mount Sinai Hospital
Marius K. Lemberg
University of Cologne
Science
École Polytechnique Fédérale de Lausanne
ETH Zurich
Lunenfeld-Tanenbaum Research Institute
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Weihofen et al. (Fri,) studied this question.
synapsesocial.com/papers/69dd4f5efb7610310c101fa2 — DOI: https://doi.org/10.1126/science.1070925