Literature DB >> 20838693

Zwitterionic i-motif structures are preserved in DNA negatively charged ions produced by electrospray mass spectrometry.

Frederic Rosu1, Valérie Gabelica, Laure Joly, Gilles Grégoire, Edwin De Pauw.   

Abstract

DNA cytosine-rich strands can fold into an intercalated motif (i-motif) structure. The i-motif is formed by mutually intercalated duplexes containing proton-mediated C-H(+)-C (cytosine-proton-cytosine) base pairs. Negatively charged ions of DNA i-motifs produced by electrospray mass spectrometry are therefore zwitterionic if the base pairing motif is preserved in the gas phase. Here we used IRMPD spectroscopy and ion mobility spectrometry to assess whether i-motif structures were preserved in the gas phase. We first investigated the IRMPD spectral signature of the tetramer [dC(6)](4), which can only be formed via C-H(+)-C base pairing, compared to the single strand dC(6). The IR signature of i-motif formation is an apparent broadening of the band at 1650 cm(-1). DFT calculations show this apparent broadening is actually due to blue-shifts of the NH(2) scissoring modes and red shifts of C[double bond, length as m-dash]O stretching modes. We then investigated the gas-phase conformations of the telomeric sequence d(CCCAAT)(3)CCC, that can form an intramolecular i-motif, by performing IRMPD spectroscopy and ion mobility spectrometry as a function of the charge state. We show that the negative ions of the lowest charge states correspond to a preserved i-motif structure. This is the first demonstration of the native extraction of solution-phase zwitterionic nucleic acids using negative electrospray ionization.

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Year:  2010        PMID: 20838693     DOI: 10.1039/c0cp00782j

Source DB:  PubMed          Journal:  Phys Chem Chem Phys        ISSN: 1463-9076            Impact factor:   3.676


  7 in total

1.  Gas-phase structure of amyloid-β (12-28) peptide investigated by infrared spectroscopy, electron capture dissociation and ion mobility mass spectrometry.

Authors:  Thi Nga Le; Jean Christophe Poully; Frédéric Lecomte; Nicolas Nieuwjaer; Bruno Manil; Charles Desfrançois; Fabien Chirot; Jerome Lemoine; Philippe Dugourd; Guillaume van der Rest; Gilles Grégoire
Journal:  J Am Soc Mass Spectrom       Date:  2013-09-17       Impact factor: 3.109

2.  Base-Pairing Energies of Protonated Nucleoside Base Pairs of dCyd and m(5)dCyd: Implications for the Stability of DNA i-Motif Conformations.

Authors:  Bo Yang; M T Rodgers
Journal:  J Am Soc Mass Spectrom       Date:  2015-05-22       Impact factor: 3.109

3.  Base-Pairing Energies of Proton-Bound Dimers and Proton Affinities of 1-Methyl-5-Halocytosines: Implications for the Effects of Halogenation on the Stability of the DNA i-Motif.

Authors:  Bo Yang; R R Wu; M T Rodgers
Journal:  J Am Soc Mass Spectrom       Date:  2015-07-07       Impact factor: 3.109

4.  Formation and Dissociation of the Interstrand i-Motif by the Sequences d(XnC 4Y m) Monitored with Electrospray Ionization Mass Spectrometry.

Authors:  Yanwei Cao; Yujiao Qin; Michael Bruist; Shang Gao; Bing Wang; Huixin Wang; Xinhua Guo
Journal:  J Am Soc Mass Spectrom       Date:  2015-04-11       Impact factor: 3.109

5.  Structures of the kinetically trapped i-motif DNA intermediates.

Authors:  Alyssa Garabedian; David Butcher; Jennifer L Lippens; Jaroslava Miksovska; Prem P Chapagain; Daniele Fabris; Mark E Ridgeway; Melvin A Park; Francisco Fernandez-Lima
Journal:  Phys Chem Chem Phys       Date:  2016-09-29       Impact factor: 3.676

Review 6.  Recent developments in the characterization of nucleic acids by liquid chromatography, capillary electrophoresis, ion mobility, and mass spectrometry (2010-2020).

Authors:  Inês C Santos; Jennifer S Brodbelt
Journal:  J Sep Sci       Date:  2020-10-15       Impact factor: 3.645

7.  Synthesis and structural characterization of stable branched DNA g-quadruplexes using the trebler phosphoramidite.

Authors:  Rubén Ferreira; Margarita Alvira; Anna Aviñó; Irene Gómez-Pinto; Carlos González; Valérie Gabelica; Ramon Eritja
Journal:  ChemistryOpen       Date:  2012-04       Impact factor: 2.911

  7 in total

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