Startseite Molecular contortionism – on the physical limits of serpin ‘loop-sheet’ polymers
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Molecular contortionism – on the physical limits of serpin ‘loop-sheet’ polymers

  • James A. Huntington und James C. Whisstock
Veröffentlicht/Copyright: 19. Mai 2010
Biological Chemistry
Aus der Zeitschrift Band 391 Heft 8

Abstract

Members of the serpin (serine protease inhibitor) superfamily fold into a metastable conformation that is crucial for proper function. As a consequence, serpins are susceptible to mutations that cause misfolding and the intracellular accumulation of pathogenic polymers. The mechanism of serpin polymerisation remains to be resolved, however, over the past two decades the ‘loop-sheet’ hypothesis has gained wide acceptance. In this mechanism the reactive centre loop of one serpin monomer inserts into the β-sheet A of another (in trans), in a manner similar to what is seen for reactive centre loop-cleaved and latent conformations (in cis). The hypothesis has been refined in response to certain experimental data, but it has proved difficult to assess the various propositions without creating molecular models. Here we evaluate the loop-sheet mechanism by creating models of pentamers of the archetypal serpin α1-antitrypsin. We conclude that an inescapable consequence of the loop-sheet mechanism is polymer compaction and rigidity, properties that are inconsistent with the ‘beads-on-a-string’ morphology of polymers obtained from human tissue. The recent crystal structure of a domain-swapped serpin dimer suggests an alternative mechanism that is consistent with known polymer properties, including the requirement of partial unfolding to induce polymer formation in vitro, and polymerisation from a folding intermediate in vivo.


Corresponding author

Received: 2010-3-10
Accepted: 2010-4-1
Published Online: 2010-05-19
Published in Print: 2010-08-01

©2010 by Walter de Gruyter Berlin New York

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  9. Proteolysis of platelet receptors in humans and other species
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  12. Nuclear cysteine cathepsin variants in thyroid carcinoma cells
  13. Deletion of cathepsin H perturbs angiogenic switching, vascularization and growth of tumors in a mouse model of pancreatic islet cell cancer
  14. Cathepsin E enhances anticancer activity of doxorubicin on human prostate cancer cells showing resistance to TRAIL-mediated apoptosis
  15. Hydrophilic residues surrounding the S1 and S2 pockets contribute to dimerisation and catalysis in human dipeptidyl peptidase 8 (DP8)
  16. Molecular contortionism – on the physical limits of serpin ‘loop-sheet’ polymers
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Heruntergeladen am 6.11.2025 von https://www.degruyterbrill.com/document/doi/10.1515/bc.2010.085/html
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