Literature DB >> 19007897

Structure and function of gamma-secretase.

Alexandra Tolia1, Bart De Strooper.   

Abstract

The gamma-secretase complex is a prime target for pharmacological intervention in Alzheimer's disease and so far drug discovery efforts have yielded a large variety of potent and rather specific inhibitors of this enzymatic activity. However, as gamma-secretase is able to cleave a wide variety of physiological important substrates, the real challenge is to develop substrate-specific compounds. Therefore, obtaining structural information about gamma-secretase is indispensable. As crystal structures of the complex will be difficult to achieve, applied biochemical approaches need to be integrated with structural information obtained from other intramembrane-cleaving proteases. Here we review current knowledge about the structure and function of gamma-secretase and discuss the value of these findings for the mechanistic understanding of this unusual protease.

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Year:  2008        PMID: 19007897     DOI: 10.1016/j.semcdb.2008.10.007

Source DB:  PubMed          Journal:  Semin Cell Dev Biol        ISSN: 1084-9521            Impact factor:   7.727


  30 in total

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Journal:  Development       Date:  2011-12-21       Impact factor: 6.868

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Review 3.  Therapeutic approaches to modulating Notch signaling: current challenges and future prospects.

Authors:  Casper Groth; Mark E Fortini
Journal:  Semin Cell Dev Biol       Date:  2012-01-30       Impact factor: 7.727

Review 4.  How intramembrane proteases bury hydrolytic reactions in the membrane.

Authors:  Elinor Erez; Deborah Fass; Eitan Bibi
Journal:  Nature       Date:  2009-05-21       Impact factor: 49.962

5.  Identification of a tetratricopeptide repeat-like domain in the nicastrin subunit of γ-secretase using synthetic antibodies.

Authors:  Xulun Zhang; Robert J Hoey; Guoqing Lin; Akiko Koide; Brenda Leung; Kwangwook Ahn; Georgia Dolios; Marcin Paduch; Takeshi Ikeuchi; Rong Wang; Yue-Ming Li; Shohei Koide; Sangram S Sisodia
Journal:  Proc Natl Acad Sci U S A       Date:  2012-05-14       Impact factor: 11.205

6.  Attenuated Abeta42 responses to low potency gamma-secretase modulators can be overcome for many pathogenic presenilin mutants by second-generation compounds.

Authors:  Benedikt Kretner; Akio Fukumori; Amelie Gutsmiedl; Richard M Page; Thomas Luebbers; Guido Galley; Karlheinz Baumann; Christian Haass; Harald Steiner
Journal:  J Biol Chem       Date:  2011-02-25       Impact factor: 5.157

7.  Beta-amyloid precursor protein mutants respond to gamma-secretase modulators.

Authors:  Richard M Page; Amelie Gutsmiedl; Akio Fukumori; Edith Winkler; Christian Haass; Harald Steiner
Journal:  J Biol Chem       Date:  2010-03-26       Impact factor: 5.157

8.  Signature amyloid β profiles are produced by different γ-secretase complexes.

Authors:  Hermien Acx; Lucía Chávez-Gutiérrez; Lutgarde Serneels; Sam Lismont; Manasi Benurwar; Nadav Elad; Bart De Strooper
Journal:  J Biol Chem       Date:  2013-12-13       Impact factor: 5.157

9.  DC2 and keratinocyte-associated protein 2 (KCP2), subunits of the oligosaccharyltransferase complex, are regulators of the gamma-secretase-directed processing of amyloid precursor protein (APP).

Authors:  Cornelia M Wilson; Amandine Magnaudeix; Catherine Yardin; Faraj Terro
Journal:  J Biol Chem       Date:  2011-07-18       Impact factor: 5.157

10.  Identification of an archaeal presenilin-like intramembrane protease.

Authors:  Celia Torres-Arancivia; Carolyn M Ross; Jose Chavez; Zahra Assur; Georgia Dolios; Filippo Mancia; Iban Ubarretxena-Belandia
Journal:  PLoS One       Date:  2010-09-29       Impact factor: 3.240

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