Members of the serpin (serine proteinase inhibitor) superfamily play a central role in the control of inflammatory, coagulation, and fibrinolytic cascades. Point mutations that cause abnormal conformational transitions in these proteins can trigger disease. Recent work has defined three pathways by which these conformers cause tissue damage. Here, we describe how these three mechanisms can be integrated into a new model of the pathogenesis of emphysema caused by mutations in the serpin α1-antitrypsin
Serpins have a central role in regulating proteolysis in blood coagulation, fibrinolysis, and inflam...
Protease inhibitors of the serpin family are characterised by a metastable native fold which is nece...
Alpha-1-antitrypsin (alpha(1)-antitrypsin) is the archetypal member of the serine proteinase inhibit...
Point mutations cause members of the serine protease inhibitor (serpin) superfamily to undergo a nov...
α-Antitrypsin is the prototypical member of the serine proteinase inhibitor or serpin superfamily of...
The serpinopathies result from point mutations in members of the serine protease inhibitor or serpin...
α1-Antitrypsin is the prototypical member of the serine proteinase inhibitor or serpin superfamily o...
Excessive enzyme activity often has pathological consequences. This for example is the case in throm...
The serpinopathies result from point mutations in members of the serine protease inhibitor or serpin...
AbstractSerine proteinase inhibitors (Serpins) are irreversible suicide inhibitors of proteases that...
Protein misfolding is associated with a range of diseases and occurs when a protein meanders from it...
AbstractAlpha1-antitrypsin deficiency results from point mutations that distort the structure of the...
The serpinopathies result from the ordered polymerization of mutants of members of the serine protei...
The serpinopathies result from the ordered polymerization of mutants of members of the serine protei...
Our current knowledge about the cellular mechanisms underlying serpin-related disorders, the serpino...
Serpins have a central role in regulating proteolysis in blood coagulation, fibrinolysis, and inflam...
Protease inhibitors of the serpin family are characterised by a metastable native fold which is nece...
Alpha-1-antitrypsin (alpha(1)-antitrypsin) is the archetypal member of the serine proteinase inhibit...
Point mutations cause members of the serine protease inhibitor (serpin) superfamily to undergo a nov...
α-Antitrypsin is the prototypical member of the serine proteinase inhibitor or serpin superfamily of...
The serpinopathies result from point mutations in members of the serine protease inhibitor or serpin...
α1-Antitrypsin is the prototypical member of the serine proteinase inhibitor or serpin superfamily o...
Excessive enzyme activity often has pathological consequences. This for example is the case in throm...
The serpinopathies result from point mutations in members of the serine protease inhibitor or serpin...
AbstractSerine proteinase inhibitors (Serpins) are irreversible suicide inhibitors of proteases that...
Protein misfolding is associated with a range of diseases and occurs when a protein meanders from it...
AbstractAlpha1-antitrypsin deficiency results from point mutations that distort the structure of the...
The serpinopathies result from the ordered polymerization of mutants of members of the serine protei...
The serpinopathies result from the ordered polymerization of mutants of members of the serine protei...
Our current knowledge about the cellular mechanisms underlying serpin-related disorders, the serpino...
Serpins have a central role in regulating proteolysis in blood coagulation, fibrinolysis, and inflam...
Protease inhibitors of the serpin family are characterised by a metastable native fold which is nece...
Alpha-1-antitrypsin (alpha(1)-antitrypsin) is the archetypal member of the serine proteinase inhibit...