| Literature DB >> 24161741 |
M Wysocka1, N Gruba1, A Miecznikowska1, J Popow-Stellmaszyk1, M Gütschow2, M Stirnberg2, N Furtmann3, J Bajorath4, A Lesner5, K Rolka1.
Abstract
Human matriptase-2 is an enzyme that belongs to the family of type II transmembrane serine proteases. So far there is a limited knowledge regarding its specificity and protein substrate(s). One of the identified natural substrates is hemojuvelin, a protein involved in the control of iron homeostasis. In this work, we describe the synthesis and evaluation of internal quenched substrates using a combinatorial approach. The iterative deconvolution of two libraries to define the specificity of matriptase-2 yielded to the identification of the substrate ABZ-Ile-Arg-Ala-Arg-Ser-Ala-Gly-Tyr(3-NO2)-NH2 with a k(cat)/K(m) value of 4.5 × 10(5) M(-1) × s(-1), i.e. the highest specificity constant reported so far for matriptase-2.Entities:
Keywords: Combinatorial chemistry; Fluorogenic substrates; Internally quenched substrates; Matriptase-2
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Year: 2013 PMID: 24161741 DOI: 10.1016/j.biochi.2013.10.001
Source DB: PubMed Journal: Biochimie ISSN: 0300-9084 Impact factor: 4.079