help button home button
AJRCMB
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS

Published ahead of print on March 11, 2004, doi:10.1165/rcmb.2003-0276OC
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
2003-0276OCv1
31/2/133    most recent
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Parfrey, H.
Right arrow Articles by Mahadeva, R.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Parfrey, H.
Right arrow Articles by Mahadeva, R.
American Journal of Respiratory Cell and Molecular Biology. Vol. 31, pp. 133-139, 2004
© 2004 American Thoracic Society
DOI: 10.1165/rcmb.2003-0276OC

Inhibiting Polymerization

New Therapeutic Strategies for Z {alpha}1-Antitrypsin–Related Emphysema

Helen Parfrey, Timothy R. Dafforn, Didier Belorgey, David A. Lomas and Ravi Mahadeva

Division of Respiratory Medicine, Department of Medicine, University of Cambridge, Cambridge Institute for Medical Research, Cambridge, United Kingdom

Address correspondence to: Helen Parfrey, Division of Respiratory Medicine, Department of Medicine, University of Cambridge, Cambridge Institute for Medical Research, MRC/Wellcome Trust Building, Hills Road, Cambridge CB2 2XY, UK. E-mail: hp226{at}cam.ac.uk

The Z variant of {alpha}1-antitrypsin (Z-AT) is present in 4% of Northern Europeans and is associated with liver cirrhosis and emphysema. Polymers accumulate within the hepatocyte and the subsequent plasma deficiency of AT renders the lungs susceptible to proteolysis and early onset emphysema. We have previously demonstrated that the Phe-Leu-Glu-Ala-Ile-Gly (6 mer) peptide specifically binds to Z-AT and inhibits polymerization. Here we present the first detailed biochemical study of the purified Z-AT-6 mer binary complex. Biochemical studies indicated that this complex was inactive as a proteinase inhibitor and the peptide annealed to ß-sheet A of Z-AT. Removal of the N-acetyl terminus of the 6 mer peptide did not affect the peptide's ability to prevent polymer formation. However, the nonacetylated 6 mer–Z-AT complex dissociated at a rate 2.75x faster than the acetylated 6 mer–Z-AT complex to yield an active inhibitor; Koff 5.5 ± 1.07 versus 2.0 ± 0.25 106 s–1, respectively. These biochemical data indicate a potential therapeutic approach whereby polymerization is prevented in the liver, with the gradual release of the peptide from the binary complex restoring proteinase inhibitory function within the tissues. Thus, it raises the novel prospect of ameliorating both the cirrhosis and the emphysema associated with Z-AT.

Abbreviations: {alpha}1-antitrypsin, AT • acetylated 6 mer peptide, Ac-6 mer • nonacetylated 6 mer peptide, non-Ac-6 mer • acetylated 12 mer peptide, Ac-12 mer • binary complex, BC • Z variant of {alpha}1-antitrypsin, Z-AT




This article has been cited by other articles:


Home page
Am. J. Respir. Cell Mol. Bio.Home page
Y.-P. Chang, R. Mahadeva, W.-S. W. Chang, A. Shukla, T. R. Dafforn, and Y.-H. Chu
Identification of a 4-mer Peptide Inhibitor that Effectively Blocks the Polymerization of Pathogenic Z {alpha}1-Antitrypsin
Am. J. Respir. Cell Mol. Biol., November 1, 2006; 35(5): 540 - 548.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Proc. Am. Thorac. Soc. Am. J. Respir. Crit. Care Med.
Copyright © 2004 American Thoracic Society.
  Membership Renewal