000			02305 am a22002533u 4500
042			_adc
100	1	0	_aKay, Richard G. _eauthor
700	1	0	_aForeman, Rachel E. _eauthor
700	1	0	_aRoberts, Geoff P. _eauthor _92971
700	1	0	_aHardwick, Richard _eauthor _92972
700	1	0	_aReimann, Frank _eauthor
700	1	0	_aGribble, Fiona M. _eauthor
245	0	0	_aMass spectrometric characterisation of the circulating peptidome following oral glucose ingestion in control and gastrectomised patients
260			_c2020-09-30.
500			_a/pmc/articles/PMC7614168/
500			_a/pubmed/32492232
520			_aMeal ingestion triggers secretion of a variety of gut and endocrine peptides, several of which are routinely measured in research studies by commercial immunoassays. We developed an LC-MS/MS based assay for parallel monitoring of multiple peptides in small volumes of human plasma, providing the benefit of analysing exact peptide sequences rather than immuno-reactivity, and potential advantages of cost and sample volumes for measuring multiple hormones. The method involves acetonitrile precipitation of larger proteins, followed by solid phase extraction and nano-LC-MS/MS using an untargeted approach on an orbitrap mass spectrometer. Application of the method to human plasma from control subjects and patients who have undergone gastrectomy with Roux-en-Y reconstruction, revealed elevated levels of a number of gut peptides following glucose ingestion, including GLP-1(7-36), GLP-1(9-36), glicentin, oxyntomodulin, GIP(1-42), GIP(3-42), PYY(1-36), PYY(3-36), neurotensin, insulin and C-peptide, as well as motilin, which fell following glucose ingestion. Results showed good correlation with those hormones measured previously by immunoassay in the same samples. The gastrectomy group had higher, but non-glucose-dependent, circulating levels of peptides from PIGR and DMBT1. Overall, the method is fast, generic, reproducible and inexpensive, and requires only small plasma samples, making it potentially adaptable for multiplexed measurement of a variety of plasma peptides.
540			_a
546			_aen
690			_aArticle
655	7		_aText _2local
786	0		_nRapid Commun Mass Spectrom
856	4	1	_uhttp://dx.doi.org/10.1002/rcm.8849 _zConnect to this object online.
999			_c2304 _d2304