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Characterization of SPINK9, a KLK5-specific inhibitor expressed in palmo-plantar epidermis
Umeå University, Faculty of Medicine, Department of Medical Biochemistry and Biophysics.
Umeå University, Faculty of Science and Technology, Department of Chemistry.
Umeå University, Faculty of Medicine, Department of Molecular Biology (Faculty of Medicine).
Umeå University, Faculty of Medicine, Department of Medical Biochemistry and Biophysics.
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2012 (English)In: Biological chemistry (Print), ISSN 1431-6730, E-ISSN 1437-4315, Vol. 393, no 5, 369-377 p.Article in journal (Refereed) Published
Abstract [en]

SPINK9, a Kazal-type serine protease inhibitor, is almost exclusively expressed in the palmo-plantar epidermis. SPINK9 selectively inhibits kallikrein-related peptidase 5 (KLK5), no other target enzyme is known at present. In this study, we defined the reactive loop to residues 48 and 49 of SPINK9 and characterized the inhibition and binding of different SPINK9 variants towards KLK5, KLK7, KLK8 and KLK14. Substitutions of single amino acids in the reactive loop had a large impact on both inhibitory efficiency and specificity. Binding studies showed that it is mainly the dissociation rate that is affected by the amino acid substitutions. The inhibitory effect of wild-type SPINK9 was clearly pH-dependent with an improved effect at a pH similar to that of the outer layers of the skin. Modeling of the enzyme-inhibitor complexes showed that the reactive loop of SPINK9 fits very well into the deep negatively charged binding pocket of KLK5. A decrease in pH protonates His48 of the wild-type protein resulting in a positively charged residue, thereby explaining the observed decreased dissociation rate. Interestingly, substitution with a positively charged amino acid at position 48 resulted in a more efficient inhibitor at higher pH.

Place, publisher, year, edition, pages
Walter de Gruyter, 2012. Vol. 393, no 5, 369-377 p.
Keyword [en]
binding studies, inhibition, kallikrein-related peptidases, Kazal-type inhibitor, KLK5, SPINK9
National Category
Cell and Molecular Biology
URN: urn:nbn:se:umu:diva-56422DOI: 10.1515/hsz-2011-0238ISI: 000304334100007OAI: diva2:535013
Available from: 2012-06-19 Created: 2012-06-18 Last updated: 2016-08-22Bibliographically approved

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Brännström, KristofferÖhman, Andersvon Pawel-Rammingen, UlrichOlofsson, AndersBrattsand, Maria
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Department of Medical Biochemistry and BiophysicsDepartment of ChemistryDepartment of Molecular Biology (Faculty of Medicine)Dermatology and Venerology
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