Rapid Screening and Identification of New Soluble Tannin-Salivary Protein Aggregates in Saliva by Mass Spectrometry (MALDI-TOF-TOF and FIA-ESI-MS)

• Tipo: Artigo em Revista Científica Internacional
• Data: 2014

Autores

Perez Gregorio, MR (Autor) Outra; Mateus, N (Autor) FCUP; de Freitas, V (Autor) Outra

Revista

Título: Langmuir

Vol. 30

Páginas: 8528-8537

ISSN: 0743-7463

Editora: American Chemical Society

Indexação

ISI Web of Knowledge - 33 Citações

Scopus - 35 Citações

Classificação Científica

FOS: Ciências da engenharia e tecnologias > Engenharia dos materiais

Outras Informações

ID Authenticus: P-009-MSK

DOI: 10.1021/la502184f

Abstract (EN): Astringency is mainly attributed to the interaction between tannins and salivary proteins. Proline-rich proteins, histatins, and statherins are supposed to be the most reactive salivary proteins. This study aims to contribute to the knowledge of the tannin protein binding process in saliva. It was identified for the first time in several soluble tannin human salivary protein aggregates. A rapid mass spectrometry analytical method (MALDI-TOF and FIA-ESI-MS) was developed to identify new soluble tannin human salivary protein aggregates. Three different tannins procyanidin B3 (B3), procyanidin B2 gallate (B2G), and pentagalloylglucoside (PGG)-were tested to elucidate the tannin selectivity toward histatins, proline-rich proteins, and statherins in human saliva. A greater number of aggregates with a higher molecular weight was found when PGG was tested while no difference in the number and molecular mass range was observed in B3 or B2G salivary protein aggregates. This study confirms for the first time the bilateral selectivity of tannins and protein to yield soluble tannin human salivary protein complexes. The results confirm that B3 and B2G are more selective than PGG. Furthermore, the families of proteins involved in the majority of B3 salivary protein soluble aggregates were primarly histatins, followed by basic proline-rich proteins and statherins. When B2G was tested, basic proline-rich proteins were involved in a greater number of aggregates, followed by histatines and statherins. Basic proline-rich proteins were also the family of proteins that formed a greater number of PGG salivary protein aggregates followed by statherins and histatins. Acidic proline-rich proteins and glucosilated proline-rich proteins formed fewer soluble aggregates regardless of the tannin tested. The aggregation process was also found to be influenced by tannin and protein polarity. Indeed, the protein/tannin ratio of soluble aggregates increased with the tannin polarity. On the other hand, the only amphiphilic salivary proteins studied (histatins) formed a greater number of aggregates with the least polar tannin tested (B3).

Idioma: Inglês

Tipo (Avaliação Docente): Científica