{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,11,11]],"date-time":"2025-11-11T12:55:29Z","timestamp":1762865729809,"version":"build-2065373602"},"reference-count":28,"publisher":"Wiley","issue":"20","license":[{"start":{"date-parts":[[2010,9,29]],"date-time":"2010-09-29T00:00:00Z","timestamp":1285718400000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":["analyticalsciencejournals.onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Proteomics"],"published-print":{"date-parts":[[2010,10]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>Proline\u2010rich proteins (PRPs) are the most complex family of salivary peptides with distinct isoforms and PTMs. Up to date, only the serine phosphorylation at positions 8, 17, and 22 have been experimentally observed on acidic PRP (aPRPs), and at position 8 on basic PRP1 and 2. The presence of a glucoronyl group at Ser17 was also noticed on aPRP. The main goal of this study was to identify new PTMs and distinct isoforms of salivary PRPs using LC\u2010MALDI\u2010TOF\/TOF. Through the salivary peptidome characterization of 20 different subjects from Control, Diabetic, and Head and Neck Cancer groups, it was possible to identify the following species: (i) <jats:italic>N<\/jats:italic>\u2010glycosylation sites: two in basic proline\u2010rich protein 2 (bPRP2), one in bPRP3 and one in bPRP4; (ii) <jats:italic>O<\/jats:italic>\u2010glycosylation sites: two in bPRP2 and one in aPRP; (iii) other terminal monosaccharide sites: six in bPRP1, two in bPRP2 and two in bPRP3; (iv) other modifications such as <jats:italic>N<\/jats:italic>\u2010terminal pyro\u2010Glu (two in bPRP1, six in bPRP2, eight in bPRP3 and nine in bPRP4); (v) phosphorylation in serine, three in bPRP1, one in bPRP2, one in bPRP3 and one in aPRP1; (vi) bPRP1 (allele S, allele M and variant CP5) and bPRP4 (allele M). In summary, salivary peptidome data analysis allowed the identification of 45 new PRP\u2010modified residues, mainly due to glycosylation, phosphorylation and conversion of Gln to pyro\u2010Glu. Moreover, comparing all subject groups, it was noticed a predominance of <jats:italic>N<\/jats:italic>\u2010acetyl hexosamine modification on bPRPs in the Head and Neck Cancer patients.<\/jats:p>","DOI":"10.1002\/pmic.201000261","type":"journal-article","created":{"date-parts":[[2010,9,29]],"date-time":"2010-09-29T05:43:09Z","timestamp":1285738989000},"page":"3732-3742","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":40,"title":["Finding new posttranslational modifications in salivary proline\u2010rich proteins"],"prefix":"10.1002","volume":"10","author":[{"given":"Rui","family":"Vitorino","sequence":"first","affiliation":[]},{"given":"Renato","family":"Alves","sequence":"additional","affiliation":[]},{"given":"Ant\u00f3nio","family":"Barros","sequence":"additional","affiliation":[]},{"given":"Armando","family":"Caseiro","sequence":"additional","affiliation":[]},{"given":"Rita","family":"Ferreira","sequence":"additional","affiliation":[]},{"given":"Maria Calheiros","family":"Lobo","sequence":"additional","affiliation":[]},{"given":"Ana","family":"Bastos","sequence":"additional","affiliation":[]},{"given":"Jos\u00e9","family":"Duarte","sequence":"additional","affiliation":[]},{"given":"Davide","family":"Carvalho","sequence":"additional","affiliation":[]},{"given":"L\u00facio Lara","family":"Santos","sequence":"additional","affiliation":[]},{"given":"Francisco L.","family":"Amado","sequence":"additional","affiliation":[]}],"member":"311","published-online":{"date-parts":[[2010,9,29]]},"reference":[{"key":"e_1_2_3_2_2","doi-asserted-by":"publisher","DOI":"10.1586\/14789450.2.4.521"},{"key":"e_1_2_3_3_2","doi-asserted-by":"publisher","DOI":"10.1177\/154405910708600802"},{"key":"e_1_2_3_4_2","doi-asserted-by":"publisher","DOI":"10.1002\/pmic.200600284"},{"key":"e_1_2_3_5_2","doi-asserted-by":"publisher","DOI":"10.1007\/s10989-007-9109-9"},{"key":"e_1_2_3_6_2","doi-asserted-by":"publisher","DOI":"10.1021\/bi00228a001"},{"key":"e_1_2_3_7_2","doi-asserted-by":"publisher","DOI":"10.1007\/BF00223503"},{"key":"e_1_2_3_8_2","doi-asserted-by":"publisher","DOI":"10.1074\/mcp.M700501-MCP200"},{"key":"e_1_2_3_9_2","doi-asserted-by":"publisher","DOI":"10.1021\/bi00799a013"},{"key":"e_1_2_3_10_2","doi-asserted-by":"publisher","DOI":"10.1016\/S0014-5793(00)01645-8"},{"key":"e_1_2_3_11_2","doi-asserted-by":"publisher","DOI":"10.1093\/oxfordjournals.jbchem.a133900"},{"key":"e_1_2_3_12_2","doi-asserted-by":"publisher","DOI":"10.1021\/bi00268a036"},{"key":"e_1_2_3_13_2","doi-asserted-by":"crossref","first-page":"1991","DOI":"10.1093\/oxfordjournals.jbchem.a134553","article-title":"Further fractionation of basic proline\u2010rich peptides from human parotid saliva and complete amino acid sequence of basic proline\u2010rich peptide P\u2010H","volume":"94","author":"Saitoh E.","year":"1983","journal-title":"J. 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