Literature DB >> 19189970

Intramembrane proteolysis by signal peptide peptidases: a comparative discussion of GXGD-type aspartyl proteases.

Regina Fluhrer1, Harald Steiner, Christian Haass.   

Abstract

Intramembrane-cleaving proteases are required for reverse signaling and membrane protein degradation. A major class of these proteases is represented by the GXGD-type aspartyl proteases. GXGD describes a novel signature sequence that distinguishes these proteases from conventional aspartyl proteases. Members of the family of the GXGD-type aspartyl proteases are the Alzheimer disease-related gamma-secretase, the signal peptide peptidases and their homologs, and the bacterial type IV prepilin peptidases. We will describe the major biochemical and functional properties of the signal peptide peptidases and their relatives. We then compare these properties with those of gamma-secretase and discuss common mechanisms but also point out a number of substantial differences.

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Year:  2009        PMID: 19189970      PMCID: PMC2682845          DOI: 10.1074/jbc.R800040200

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  45 in total

1.  Requirements for presenilin-dependent cleavage of notch and other transmembrane proteins.

Authors:  G Struhl; A Adachi
Journal:  Mol Cell       Date:  2000-09       Impact factor: 17.970

2.  Intramembrane proteolysis of signal peptides: an essential step in the generation of HLA-E epitopes.

Authors:  M K Lemberg; F A Bland; A Weihofen; V M Braud; B Martoglio
Journal:  J Immunol       Date:  2001-12-01       Impact factor: 5.422

3.  A subset of NSAIDs lower amyloidogenic Abeta42 independently of cyclooxygenase activity.

Authors:  S Weggen; J L Eriksen; P Das; S A Sagi; R Wang; C U Pietrzik; K A Findlay; T E Smith; M P Murphy; T Bulter; D E Kang; N Marquez-Sterling; T E Golde; E H Koo
Journal:  Nature       Date:  2001-11-08       Impact factor: 49.962

4.  Activity-dependent isolation of the presenilin- gamma -secretase complex reveals nicastrin and a gamma substrate.

Authors:  William P Esler; W Taylor Kimberly; Beth L Ostaszewski; Wenjuan Ye; Thekla S Diehl; Dennis J Selkoe; Michael S Wolfe
Journal:  Proc Natl Acad Sci U S A       Date:  2002-02-26       Impact factor: 11.205

5.  Requirements for signal peptide peptidase-catalyzed intramembrane proteolysis.

Authors:  Marius K Lemberg; Bruno Martoglio
Journal:  Mol Cell       Date:  2002-10       Impact factor: 17.970

6.  The type 4 prepilin peptidases comprise a novel family of aspartic acid proteases.

Authors:  C F LaPointe; R K Taylor
Journal:  J Biol Chem       Date:  2000-01-14       Impact factor: 5.157

7.  Release of signal peptide fragments into the cytosol requires cleavage in the transmembrane region by a protease activity that is specifically blocked by a novel cysteine protease inhibitor.

Authors:  A Weihofen; M K Lemberg; H L Ploegh; M Bogyo; B Martoglio
Journal:  J Biol Chem       Date:  2000-10-06       Impact factor: 5.157

8.  Presenilin-1 mutations of leucine 166 equally affect the generation of the Notch and APP intracellular domains independent of their effect on Abeta 42 production.

Authors:  Tobias Moehlmann; Edith Winkler; Xuefeng Xia; Dieter Edbauer; Jill Murrell; Anja Capell; Christoph Kaether; Hui Zheng; Bernardino Ghetti; Christian Haass; Harald Steiner
Journal:  Proc Natl Acad Sci U S A       Date:  2002-06-04       Impact factor: 11.205

9.  Identification of a novel family of presenilin homologues.

Authors:  Chris P Ponting; Mike Hutton; Andrew Nyborg; Matthew Baker; Karen Jansen; Todd E Golde
Journal:  Hum Mol Genet       Date:  2002-05-01       Impact factor: 6.150

10.  Identification of signal peptide peptidase, a presenilin-type aspartic protease.

Authors:  Andreas Weihofen; Kathleen Binns; Marius K Lemberg; Keith Ashman; Bruno Martoglio
Journal:  Science       Date:  2002-06-21       Impact factor: 47.728

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  35 in total

1.  Three-dimensional structure of the signal peptide peptidase.

Authors:  Hiroyuki Miyashita; Yuusuke Maruyama; Hayato Isshiki; Satoko Osawa; Toshihiko Ogura; Kazuhiro Mio; Chikara Sato; Taisuke Tomita; Takeshi Iwatsubo
Journal:  J Biol Chem       Date:  2011-06-02       Impact factor: 5.157

2.  Three-amino acid spacing of presenilin endoproteolysis suggests a general stepwise cleavage of gamma-secretase-mediated intramembrane proteolysis.

Authors:  Akio Fukumori; Regina Fluhrer; Harald Steiner; Christian Haass
Journal:  J Neurosci       Date:  2010-06-09       Impact factor: 6.167

Review 3.  Membrane proteases in the bacterial protein secretion and quality control pathway.

Authors:  Ross E Dalbey; Peng Wang; Jan Maarten van Dijl
Journal:  Microbiol Mol Biol Rev       Date:  2012-06       Impact factor: 11.056

Review 4.  Intramembrane-cleaving proteases.

Authors:  Michael S Wolfe
Journal:  J Biol Chem       Date:  2009-02-03       Impact factor: 5.157

5.  Rip exposed: how ectodomain shedding regulates the proteolytic processing of transmembrane substrates.

Authors:  Daniel R Dries; Gang Yu
Journal:  Proc Natl Acad Sci U S A       Date:  2009-08-26       Impact factor: 11.205

6.  Post-liberation cleavage of signal peptides is catalyzed by the site-2 protease (S2P) in bacteria.

Authors:  Akira Saito; Yohei Hizukuri; Ei-ichi Matsuo; Shinobu Chiba; Hiroyuki Mori; Osamu Nishimura; Koreaki Ito; Yoshinori Akiyama
Journal:  Proc Natl Acad Sci U S A       Date:  2011-08-02       Impact factor: 11.205

7.  γ-Secretase Inhibitors and Modulators Induce Distinct Conformational Changes in the Active Sites of γ-Secretase and Signal Peptide Peptidase.

Authors:  Natalya Gertsik; De-Ming Chau; Yue-Ming Li
Journal:  ACS Chem Biol       Date:  2015-06-10       Impact factor: 5.100

Review 8.  Structure, mechanism and inhibition of gamma-secretase and presenilin-like proteases.

Authors:  Michael S Wolfe
Journal:  Biol Chem       Date:  2010-08       Impact factor: 3.915

9.  Proteolytic Processing of Neuregulin 1 Type III by Three Intramembrane-cleaving Proteases.

Authors:  Daniel Fleck; Matthias Voss; Ben Brankatschk; Camilla Giudici; Heike Hampel; Benjamin Schwenk; Dieter Edbauer; Akio Fukumori; Harald Steiner; Elisabeth Kremmer; Martina Haug-Kröper; Moritz J Rossner; Regina Fluhrer; Michael Willem; Christian Haass
Journal:  J Biol Chem       Date:  2015-11-16       Impact factor: 5.157

10.  Signal peptide peptidase (SPP) assembles with substrates and misfolded membrane proteins into distinct oligomeric complexes.

Authors:  Bianca Schrul; Katja Kapp; Irmgard Sinning; Bernhard Dobberstein
Journal:  Biochem J       Date:  2010-04-14       Impact factor: 3.857

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