Protomers: formation, separation and characterization via travelling wave ion mobility mass spectrometry


Autoria(s): Lalli, Priscila M.; Iglesias, Bernardo Almeida; Toma, Henrique Eisi; Sa, Gilberto F. de; Daroda, Romeu J.; Silva Filho, Juvenal C.; Szulejko, Jan E.; Araki, Koiti; Eberlin, Marcos N.
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

21/10/2013

21/10/2013

2012

Resumo

Travelling wave ion mobility mass spectrometry (TWIM-MS) with post-TWIM and pre-TWIM collision-induced dissociation (CID) experiments were used to form, separate and characterize protomers sampled directly from solutions or generated in the gas phase via CID. When in solution equilibria, these species were transferred to the gas phase via electrospray ionization, and then separated by TWIM-MS. CID performed after TWIM separation (post-TWIM) allowed the characterization of both protomers via structurally diagnostic fragments. Protonated aniline (1) sampled from solution was found to be constituted of a ca. 5:1 mixture of two gaseous protomers, that is, the N-protonated (1a) and ring protonated (1b) molecules, respectively. When dissociated, 1a nearly exclusively loses NH3, whereas 1b displays a much diverse set of fragments. When formed via CID, varying populations of 1a and 1b were detected. Two co-existing protomers of two isomeric porphyrins were also separated and characterized via post-TWIM CID. A deprotonated porphyrin sampled from a basic methanolic solution was found to be constituted predominantly of the protomer arising from deprotonation at the carboxyl group, which dissociates promptly by CO2 loss, but a CID-resistant protomer arising from deprotonation at a porphyrinic ring NH was also detected and characterized. The doubly deprotonated porphyrin was found to be constituted predominantly of a single protomer arising from deprotonation of two carboxyl groups. Copyright (C) 2012 John Wiley & Sons, Ltd.

FAPESP

FAPESP

CNPq

CNPq

FINEP

FINEP

CAPES

CAPES

Identificador

JOURNAL OF MASS SPECTROMETRY, HOBOKEN, v. 47, n. 6, pp. 712-719, JUN, 2012

1076-5174

http://www.producao.usp.br/handle/BDPI/35210

10.1002/jms.2999

http://dx.doi.org/10.1002/jms.2999

Idioma(s)

eng

Publicador

WILEY-BLACKWELL

HOBOKEN

Relação

JOURNAL OF MASS SPECTROMETRY

Direitos

closedAccess

Copyright WILEY-BLACKWELL

Palavras-Chave #PROTOMERS, PROTONATION SITE #ANILINE #PYRIDYL PORPHYRINS #ELECTROSPRAY IONIZATION #TRAVELLING WAVE ION MOBILITY #MASS SPECTROMETRY, GAS PHASE ACIDITY, GAS PHASE BASICITY #GAS-PHASE #PROTONATION SITES #PEPTIDE IONS #DRIFT-GAS #ANILINE #COMPLEXES #RING #CONFORMATION #RESOLUTION #NITROGEN #BIOCHEMICAL RESEARCH METHODS #CHEMISTRY, ANALYTICAL #SPECTROSCOPY
Tipo

article

original article

publishedVersion