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In molecular biology, elastase is an enzyme from the class of proteases (or better peptidases) that break down proteins.
There exist two genes for elastase: pancreatic (ELA-1) and neutrophil (ELA-2) elastase. From recent research, it appears that of the two, ELA-1 is not transcribed into a protein .
The neutrophil form of elastase () is 218 aminoacids long, with two asparagine-linked carbohydrate chains (see glycosylation). It is present in azurophil granules in the neutrophil cytoplasm. There appear to be two forms of neutrophil elastase, termed IIa and IIb.
Elastase breaks down elastin, an elastic fibre that—together with collagen—determines the mechanical properties of connective tissue. The neutrophil form also breaks down the Outer membrane protein A (OmpA) of E. coli and other Gram negative bacteria, and breaks down Shigella virulence factors.
The two ELA genes are located on different chromosomes:
Elastase is inhibited by the acute phase protein α1-antitryspin (A1AT), which binds covalently 1:1 to elastase. α1-antitryspin deficiency (A1AD) leads to uninhibited destruction of elastic fibre by elastase; the main result is pulmonary emphysema.
The rare disease cyclic hematopoeiesis (also called "cyclic neutropenia") is an autosomal dominant genetic disorder characterised by fluctuating neutrophil granulocyte counts over 21-day periods. During neutropenia, patients are at risk for infections. In 1999, this disease was linked to disorders in the ELA-2 gene . Other forms of congenital neutropenia also appear to be linked to ELA-2 mutations.
Neutrophil elastase is responsible for the blistering in bullous pemphigoid, a skin condition, in the presence of antibodies.