http://www.cnr.it/ontology/cnr/individuo/prodotto/ID17500
Tyrosine polysulfation of human salivary histatin 1. A post-translational modification specific of the submandibular gland (Articolo in rivista)
- Type
- Label
- Tyrosine polysulfation of human salivary histatin 1. A post-translational modification specific of the submandibular gland (Articolo in rivista) (literal)
- Anno
- 2007-01-01T00:00:00+01:00 (literal)
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- Cabras T.; Fanali C.; Monteiro J.A.; Amado F.; Inzitari R.; Desiderio C.; Scarano E.; Giardina B.; Castagnola M.; Messana I. (literal)
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- Rivista
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- ISI Web of Science (WOS) (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
- Tiziana Cabras (1), Chiara Fanali (2), Joana A. Monteiro (2,3), Francisco Amado (3), Rosanna Inzitari (2), Claudia Desiderio (4), Emanuele Scarano(5), Bruno Giardina (2), Massimo Castagnola (2) and Irene Messana (1)
(1) Department of Sciences Applied to Biosystems, Cagliari University, Cagliari, Italy
(2) Institute of Biochemistry and Clinical Biochemistry
(3) Department of Chemistry, University of Aveiro, Aveiro, Portugal
(4) Institute for the Molecular Recognition, CNR
(5)Institute of Otorhinolaryngology, Catholic University of Rome, Rome, Italy (3) Institute for the Molecular Recognition, CNR (literal)
- Titolo
- Tyrosine polysulfation of human salivary histatin 1. A post-translational modification specific of the submandibular gland (literal)
- Abstract
- Histatin 1 (His-1) derivatives showing serial mass increases of 80.0 ( 0.1 Da were detected in human
saliva by HPLC-ESI-MS. The same derivatives were also found in granules of submandibular glands
and secretions of submandibular/sublingual glands, but not in granules and secretions of parotid glands.
Only one phosphate group was present in His-1 and its derivatives, since treatment with alkaline
phosphatase provided an 80.0 Da mass decrease. His-1 derivatives were almost completely transformed
into His-1 by treatment with 1 M HCl at 100 °C, suggesting the presence of O-sulfotyrosine, which is
more labile than phospho-Tyr to acidic hydrolysis. CE-MS analysis of pronase extensive digestion of
derivatives confirmed the presence of sulfotyrosine. Derivatives were digested by trypsin, proteinase
K, and protease V-8 and analyzed by different MS strategies. The results allowed locating sulfation on
the last four tyrosines (Tyr 27, 30, 34, and 36). This study is the first report of the gland-specific sulfation
of a salivary phosphopeptide in vivo. (literal)
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