Literature DB >> 9790897

Alpha 1-antitrypsin polymerisation can occur by both loop A and C sheet mechanisms.

S P Bottomley1, P C Hopkins, J C Whisstock.   

Abstract

A number of disease states are attributable to alpha1-antitrypsin polymerisation within the endoplasmic reticulum of hepatocytes and subsequent plasma deficiency. Two distinct mechanisms describing the process of alpha1-antitrypsin polymerisation have been proposed, the loop A-sheet and C-sheet mechanisms. We report fluorescence studies using alpha1-antitrypsin covalently modified with pyrene maleimide. These results in conjunction with detailed molecular modelling studies, show that alpha1-antitrypsin is capable of undergoing both loop A-sheet and loop C-sheet mechanisms of polymerisation, depending upon the in vitro buffer conditions. Copyright 1998 Academic Press.

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Year:  1998        PMID: 9790897     DOI: 10.1006/bbrc.1998.9254

Source DB:  PubMed          Journal:  Biochem Biophys Res Commun        ISSN: 0006-291X            Impact factor:   3.575


  4 in total

1.  Structure of a serpin-enzyme complex probed by cysteine substitutions and fluorescence spectroscopy.

Authors:  J P Ludeman; J C Whisstock; P C Hopkins; B F Le Bonniec; S P Bottomley
Journal:  Biophys J       Date:  2001-01       Impact factor: 4.033

Review 2.  Engineering the serpin α1 -antitrypsin: A diversity of goals and techniques.

Authors:  Benjamin M Scott; William P Sheffield
Journal:  Protein Sci       Date:  2019-12-09       Impact factor: 6.725

3.  The human serpin proteinase inhibitor-9 self-associates at physiological temperatures.

Authors:  Lauren N Benning; James C Whisstock; Jiuru Sun; Phillip I Bird; Stephen P Bottomley
Journal:  Protein Sci       Date:  2004-07       Impact factor: 6.725

4.  Dynamic local unfolding in the serpin α-1 antitrypsin provides a mechanism for loop insertion and polymerization.

Authors:  Beena Krishnan; Lila M Gierasch
Journal:  Nat Struct Mol Biol       Date:  2011-01-23       Impact factor: 15.369

  4 in total

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