Revealing the structure of isolated peptides: IR-IR predissociation spectroscopy of protonated triglycine isomers

doi:10.1016/j.jms.2018.03.006

Title: Revealing the structure of isolated peptides: IR-IR predissociation spectroscopy of protonated triglycine isomers

Abstract

Here, we report an isomer specific IR-IR double resonance study of the mass-selected protonated triglycine peptide. Comparison of experimental spectra with calculations reveals the presence of two isomers, with protonation occurring at either the terminal amine site or one of the amide oxygen sites. The amine protonated isomer identified in our experiment contains an atypical cis amide configuration as well as a more typical trans amide. The amide protonated peptide, on the other hand, contains two trans amide moieties. Both isomers are found to be the lowest energy structures for their respective protonation site, but it is unclear, from experiments and calculations, which one is the global minimum. The presence of both in our experiments likely points to kinetic trapping of a higher energy structure. Lastly, the observed frequencies of the NH and OH stretch vibrations are used to estimate the hydrogen-bond strengths present in each isomer, accounting for the relative stabilities of these structures.

Authors:

Voss, Jonathan M. ^[1]; Fischer, Kaitlyn C. ^[1];

^[1]

Univ. of Wisconsin, Madison, WI (United States)

Publication Date:: 2018-03-08

Research Org.:: Univ. of Wisconsin-Madison, Madison, WI (United States)

Sponsoring Org.:: USDOE Office of Science (SC), Basic Energy Sciences (BES)

OSTI Identifier:: 1434665

Alternate Identifier(s):: OSTI ID: 1691641

Grant/Contract Number:: SC0010326

Resource Type:: Accepted Manuscript

Journal Name:: Journal of Molecular Spectroscopy

Additional Journal Information:: Journal Volume: 347; Journal Issue: C; Journal ID: ISSN 0022-2852

Publisher:: Elsevier

Country of Publication:: United States

Language:: English

Subject:: 37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CHEMISTRY; Infrared spectroscopy; Ions; Mass spectrometry; Peptide

Citation Formats


                    Voss, Jonathan M., Fischer, Kaitlyn C., and Garand, Etienne. Revealing the structure of isolated peptides: IR-IR predissociation spectroscopy of protonated triglycine isomers.  United States: N. p., 2018. 
        Web.  doi:10.1016/j.jms.2018.03.006.

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                    Voss, Jonathan M., Fischer, Kaitlyn C., & Garand, Etienne. Revealing the structure of isolated peptides: IR-IR predissociation spectroscopy of protonated triglycine isomers.  United States.  doi:10.1016/j.jms.2018.03.006.

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                    Voss, Jonathan M., Fischer, Kaitlyn C., and Garand, Etienne. Thu .  
        "Revealing the structure of isolated peptides: IR-IR predissociation spectroscopy of protonated triglycine isomers".  United States.  doi:10.1016/j.jms.2018.03.006.  https://www.osti.gov/servlets/purl/1434665.

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@article{osti_1434665,

  title        = {Revealing the structure of isolated peptides: IR-IR predissociation spectroscopy of protonated triglycine isomers},

  author       = {Voss, Jonathan M. and Fischer, Kaitlyn C. and Garand, Etienne},

  abstractNote = {Here, we report an isomer specific IR-IR double resonance study of the mass-selected protonated triglycine peptide. Comparison of experimental spectra with calculations reveals the presence of two isomers, with protonation occurring at either the terminal amine site or one of the amide oxygen sites. The amine protonated isomer identified in our experiment contains an atypical cis amide configuration as well as a more typical trans amide. The amide protonated peptide, on the other hand, contains two trans amide moieties. Both isomers are found to be the lowest energy structures for their respective protonation site, but it is unclear, from experiments and calculations, which one is the global minimum. The presence of both in our experiments likely points to kinetic trapping of a higher energy structure. Lastly, the observed frequencies of the NH and OH stretch vibrations are used to estimate the hydrogen-bond strengths present in each isomer, accounting for the relative stabilities of these structures.},

  doi          = {10.1016/j.jms.2018.03.006},

  journal      = {Journal of Molecular Spectroscopy},

  number       = C,

  volume       = 347,

  place        = {United States},

  year         = {2018},

  month        = {3}

}

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DOI: 10.1016/j.jms.2018.03.006

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Cited by: 5 works

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Figures / Tables:

Figure 1: An example of a neutral triglycine molecule showing the numbering scheme of N and O groups starting from the amine terminal.

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Works referencing / citing this record:

The structures and properties of anionic tryptophan complexes
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Ieritano, Christian; Featherstone, Joshua; Carr, Patrick J. J.
Physical Chemistry Chemical Physics, Vol. 20, Issue 41
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Figures/Tables have been extracted from DOE-funded journal article accepted manuscripts.

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Title: Revealing the structure of isolated peptides: IR-IR predissociation spectroscopy of protonated triglycine isomers

Abstract

Citation Formats

Figures / Tables:

The structures and properties of anionic tryptophan complexes journal, January 2018

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