| Literature DB >> 20828532 |
Mark O Palmier1, Yan G Fulcher, Steven R Van Doren.
Abstract
Elastolysis is central to progression of emphysema and aortic aneurysms. Characterization of steady-state enzyme kinetics of elastolysis is fettered by the insolubility of mature elastin and the polydispersity of solubilized elastin. We prepared a fluor-tagged, 100-kDa fraction (fEln-100) from commercial α-elastin. It is soluble, less heterogeneous in mass, cross-linked like mature elastin, and likely to retain the capacity of α-elastin to self-assemble. fEln-100 has introduced the ability to compare quantitatively the apparent k(cat) and K(m) of elastases. For example, metalloelastase (MMP-12) displays higher apparent affinity for fEln-100, while MMP-2 displays faster catalytic turnover.Entities:
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Year: 2010 PMID: 20828532 PMCID: PMC2964420 DOI: 10.1016/j.ab.2010.09.001
Source DB: PubMed Journal: Anal Biochem ISSN: 0003-2697 Impact factor: 3.365