Structure and function of SPP/SPPL proteases: insights from biochemical evidence and predictive modeling

  • More than 20 years ago, signal peptide peptidase (SPP) and its homologues, the signal peptide peptidase-like (SPPL) proteases have been identified based on their sequence similarity to presenilins, a related family of intramembrane aspartyl proteases. Other than those for the presenilins, no high-resolution structures for the SPP/SPPL proteases are available. Despite this limitation, over the years bioinformatical and biochemical data have accumulated, which altogether have provided a picture of the overall structure and topology of these proteases, their localization in the cell, the process of substrate recognition, their cleavage mechanism, and their function. Recently, the artificial intelligence-based structure prediction tool AlphaFold has added high-confidence models of the expected fold of SPP/SPPL proteases. In this review, we summarize known structural aspects of the SPP/SPPL family as well as their substrates. Of particular interest are the emerging substrate recognition andMore than 20 years ago, signal peptide peptidase (SPP) and its homologues, the signal peptide peptidase-like (SPPL) proteases have been identified based on their sequence similarity to presenilins, a related family of intramembrane aspartyl proteases. Other than those for the presenilins, no high-resolution structures for the SPP/SPPL proteases are available. Despite this limitation, over the years bioinformatical and biochemical data have accumulated, which altogether have provided a picture of the overall structure and topology of these proteases, their localization in the cell, the process of substrate recognition, their cleavage mechanism, and their function. Recently, the artificial intelligence-based structure prediction tool AlphaFold has added high-confidence models of the expected fold of SPP/SPPL proteases. In this review, we summarize known structural aspects of the SPP/SPPL family as well as their substrates. Of particular interest are the emerging substrate recognition and catalytic mechanisms that might lead to the prediction and identification of more potential substrates and deeper insight into physiological and pathophysiological roles of proteolysis.show moreshow less

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Metadaten
Author:Sabine HoeppnerGND, Bernd Schröder, Regina FluhrerORCiDGND
URN:urn:nbn:de:bvb:384-opus4-1083433
Frontdoor URLhttps://opus.bibliothek.uni-augsburg.de/opus4/108343
ISSN:1742-464XOPAC
ISSN:1742-4658OPAC
Parent Title (English):The FEBS Journal
Publisher:Wiley
Type:Article
Language:English
Year of first Publication:2023
Publishing Institution:Universität Augsburg
Release Date:2023/10/16
Tag:Cell Biology; Molecular Biology; Biochemistry
Volume:290
Issue:23
First Page:5456
Last Page:5474
DOI:https://doi.org/10.1111/febs.16968
Institutes:Fakultätsübergreifende Institute und Einrichtungen
Fakultätsübergreifende Institute und Einrichtungen / Zentrum für Interdisziplinäre Gesundheitsforschung (ZIG)
Medizinische Fakultät
Medizinische Fakultät / Lehrstuhl für Biochemie und Molekularbiologie
Dewey Decimal Classification:6 Technik, Medizin, angewandte Wissenschaften / 61 Medizin und Gesundheit / 610 Medizin und Gesundheit
Licence (German):CC-BY-NC-ND 4.0: Creative Commons: Namensnennung - Nicht kommerziell - Keine Bearbeitung (mit Print on Demand)