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Biochimie ; 97: 121-7, 2014 Feb.
Article in English | MEDLINE | ID: mdl-24161741

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.


Subject(s)
Membrane Proteins/chemistry , Molecular Docking Simulation , Oligopeptides/chemistry , Serine Endopeptidases/chemistry , Amino Acid Sequence , Catalytic Domain , HEK293 Cells , Humans , Hydrolysis , Kinetics , Membrane Proteins/biosynthesis , Membrane Proteins/isolation & purification , Molecular Sequence Data , Oligopeptides/chemical synthesis , Peptide Library , Recombinant Proteins/biosynthesis , Recombinant Proteins/chemistry , Recombinant Proteins/isolation & purification , Serine Endopeptidases/biosynthesis , Serine Endopeptidases/isolation & purification , Structure-Activity Relationship , Substrate Specificity
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