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Top-down HPLC-ESI-MS characterization of rat gliadoralin A, a new member of the family of rat submandibular gland glutamine-rich proteins and potential substrate of transglutaminase

Cabras, T. (författare)
Iavarone, F. (författare)
Pirolli, D. (författare)
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De Rosa, M. C. (författare)
Vitali, A. (författare)
Faa, G. (författare)
Cordaro, M. (författare)
Messana, I. (författare)
Ekström, Jörgen, 1944 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för neurovetenskap och fysiologi, sektionen för farmakologi,Institute of Neuroscience and Physiology, Department of Pharmacology
Castagnola, M. (författare)
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 (creator_code:org_t)
2013-05-30
2013
Engelska.
Ingår i: Journal of Separation Science. - : Wiley. - 1615-9306. ; 36:17, s. 2848-2861
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • During HPLC-ESI-MS/MS analysis of rat submandibular saliva secreted under isoprenaline stimulation, a protein with an experimental [M+H](1+) = 10544.24 m/z was detected (17.5 +/- 0.7 min). The MS/MS fragmentation pattern, manually investigated, allowed establishing an internal sequence in agreement with a DNA-derived sequence of an unknown rat protein coded D3Z9M3 (Swiss-Prot). To match the experimental MS/MS fragmentation pattern and protein mass with theoretical data, the removal from the N terminus of the signal peptide and from the C terminus of three amino acid (a.a.) residues (Arg-Ala-Val) and the cyclization of the N-terminal glutamine in pyroglutamic had to be supposed, resulting in a mature protein of 90 a.a. HPLC-ESI-MS/MS of the trypsin digest ensured 100% sequence coverage. For the high glutamine content (34/90 = 37.8%) we propose to name this protein rat gliadoralin A 1-90. Low amounts of five different isoforms were sporadically detected, which did not significantly change their relative amounts after stimulation. Gliadoralin A is substrate for transglutaminase-2, having Lys 60 and different Gln residues as major determinants for enzyme recognition. In silico investigation of superior structures evidenced that a small part of the protein adopts an -helical fold, whereas large segments are unfolded, suggesting an unordered conformation.

Ämnesord

NATURVETENSKAP  -- Kemi (hsv//swe)
NATURAL SCIENCES  -- Chemical Sciences (hsv//eng)

Nyckelord

Glutamine-rich protein
Rat
Saliva
Submandibular
Top-down
SECONDARY STRUCTURE PREDICTION
DIFFERENT PROTEOMIC PLATFORMS
HUMAN
SALIVARY PROTEOME
MASS-SPECTROMETRY
CROSS-LINKING
TISSUE
TRANSGLUTAMINASE
SERVER
EXPRESSION
PEPTIDES
PELLICLE
RELS L
1990
ARCHIVES OF ORAL BIOLOGY
V35
P1
ATES OF AMERICA
V87
P8472
RELS L
1987
JOURNAL OF BIOLOGICAL CHEMISTRY
V262
P7289

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