Elastase



         


In molecular biology, elastase is an enzyme from the class of proteases (or better peptidases) that break down proteins.

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Forms and classification

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.

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Function

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.

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Genetics

The two ELA genes are located on different chromosomes:

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Role in disease

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A1AD

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.

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Cyclic hematopoeiesis

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.

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Other diseases

Neutrophil elastase is responsible for the blistering in bullous pemphigoid, a skin condition, in the presence of antibodies.

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Sources






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