| Literature DB >> 27416753 |
Miki Yamane1, Kayoko Sugimura1, Hiroko Kawasaki1, Hideki Tatsukawa1, Kiyotaka Hitomi2.
Abstract
Transglutaminase (TGase) catalyzes protein cross-linking reactions essential for several biological processes. In differentiating keratinocytes, TG1 (keratinocyte-type) is crucial for the cross-linking of substrate proteins required for the complete formation of the cornified envelop, a proteinaceous supermolecule located in the outermost layer of the epidermis. TG1 expressions and its substrate were induced in cultured keratinocytes at differentiation-stage specific manner. In the cultured keratinocytes, we used the TG1-specific substrate peptide, which enables the specific detection of enzymatic activity to investigate its induction patterns. As a further application of the substrate peptide, several substrate candidates of TG1 that may be essential for cornified envelope formation were identified and characterized.Entities:
Keywords: Epidermis; Keratinocyte; Transglutaminase
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Year: 2016 PMID: 27416753 DOI: 10.1016/j.bbrc.2016.07.051
Source DB: PubMed Journal: Biochem Biophys Res Commun ISSN: 0006-291X Impact factor: 3.575