Low-Energy Collisions of Protonated Enantiopure Amino Acids with Chiral Target Gases

Here we report on the gas-phase interactions between protonated enantiopure amino acids ( l - and d -enantiomers of Met, Phe, and Trp) and chiral target gases [( R )- and ( S )-2-butanol, and ( S )-1-phenylethanol] in 0.1–10.0 eV low-energy collisions. Two major processes are seen to occur over this...

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Published inJournal of the American Society for Mass Spectrometry Vol. 28; no. 12; pp. 2686 - 2691
Main Authors Kulyk, K., Rebrov, O., Ryding, M., Thomas, R. D., Uggerud, E., Larsson, M.
Format Journal Article
LanguageEnglish
Published New York Springer US 01.12.2017
Springer Nature B.V
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Online AccessGet full text
ISSN1044-0305
1879-1123
1879-1123
DOI10.1007/s13361-017-1796-7

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Abstract Here we report on the gas-phase interactions between protonated enantiopure amino acids ( l - and d -enantiomers of Met, Phe, and Trp) and chiral target gases [( R )- and ( S )-2-butanol, and ( S )-1-phenylethanol] in 0.1–10.0 eV low-energy collisions. Two major processes are seen to occur over this collision energy regime, collision-induced dissociation and ion-molecule complex formation. Both processes were found to be independent of the stereo-chemical composition of the interacting ions and targets. These data shed light on the currently debated mechanisms of gas-phase chiral selectivity by demonstrating the inapplicability of the three-point model to these interactions, at least under single collision conditions. Graphical Abstract
AbstractList Here we report on the gas-phase interactions between protonated enantiopure amino acids ( l - and d -enantiomers of Met, Phe, and Trp) and chiral target gases [( R )- and ( S )-2-butanol, and ( S )-1-phenylethanol] in 0.1–10.0 eV low-energy collisions. Two major processes are seen to occur over this collision energy regime, collision-induced dissociation and ion-molecule complex formation. Both processes were found to be independent of the stereo-chemical composition of the interacting ions and targets. These data shed light on the currently debated mechanisms of gas-phase chiral selectivity by demonstrating the inapplicability of the three-point model to these interactions, at least under single collision conditions. Graphical Abstract
Here we report on the gas-phase interactions between protonated enantiopure amino acids (L- and D-enantiomers of Met, Phe, and Trp) and chiral target gases [(R)- and (S)-2-butanol, and (S)-1-phenylethanol] in 0.1-10.0 eV low-energy collisions. Two major processes are seen to occur over this collision energy regime, collision-induced dissociation and ion-molecule complex formation. Both processes were found to be independent of the stereo-chemical composition of the interacting ions and targets. These data shed light on the currently debated mechanisms of gas-phase chiral selectivity by demonstrating the inapplicability of the three-point model to these interactions, at least under single collision conditions. Graphical Abstract.Here we report on the gas-phase interactions between protonated enantiopure amino acids (L- and D-enantiomers of Met, Phe, and Trp) and chiral target gases [(R)- and (S)-2-butanol, and (S)-1-phenylethanol] in 0.1-10.0 eV low-energy collisions. Two major processes are seen to occur over this collision energy regime, collision-induced dissociation and ion-molecule complex formation. Both processes were found to be independent of the stereo-chemical composition of the interacting ions and targets. These data shed light on the currently debated mechanisms of gas-phase chiral selectivity by demonstrating the inapplicability of the three-point model to these interactions, at least under single collision conditions. Graphical Abstract.
Here we report on the gas-phase interactions between protonated enantiopure amino acids (l- and d-enantiomers of Met, Phe, and Trp) and chiral target gases [(R)- and (S)-2-butanol, and (S)-1-phenylethanol] in 0.1–10.0 eV low-energy collisions. Two major processes are seen to occur over this collision energy regime, collision-induced dissociation and ion-molecule complex formation. Both processes were found to be independent of the stereo-chemical composition of the interacting ions and targets. These data shed light on the currently debated mechanisms of gas-phase chiral selectivity by demonstrating the inapplicability of the three-point model to these interactions, at least under single collision conditions.
Here we report on the gas-phase interactions between protonated enantiopure amino acids (L- and D-enantiomers of Met, Phe, and Trp) and chiral target gases [(R)- and (S)-2-butanol, and (S)-1-phenylethanol] in 0.1-10.0 eV low-energy collisions. Two major processes are seen to occur over this collision energy regime, collision-induced dissociation and ion-molecule complex formation. Both processes were found to be independent of the stereo-chemical composition of the interacting ions and targets. These data shed light on the currently debated mechanisms of gas-phase chiral selectivity by demonstrating the inapplicability of the three-point model to these interactions, at least under single collision conditions. Graphical Abstract.
Author Uggerud, E.
Rebrov, O.
Kulyk, K.
Larsson, M.
Thomas, R. D.
Ryding, M.
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Issue 12
Keywords Gas-phase complexes
Collision induced dissociation
Enantiopure amino acids
Chiral target gases
Chirality
Low-energy collisions
Language English
License Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
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Snippet Here we report on the gas-phase interactions between protonated enantiopure amino acids ( l - and d -enantiomers of Met, Phe, and Trp) and chiral target gases...
Here we report on the gas-phase interactions between protonated enantiopure amino acids (L- and D-enantiomers of Met, Phe, and Trp) and chiral target gases...
Here we report on the gas-phase interactions between protonated enantiopure amino acids (l- and d-enantiomers of Met, Phe, and Trp) and chiral target gases...
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StartPage 2686
SubjectTerms Amino acids
Analytical Chemistry
Bioinformatics
Biotechnology
Butanol
Chemistry
Chemistry and Materials Science
Chiral target gases
Chirality
Collision induced dissociation
Collisions
Complex formation
Enantiomers
Enantiopure amino acids
Energy of dissociation
fysik
Gas-phase complexes
Low-energy collisions
Mass spectrometry
Organic Chemistry
Physics
Proteomics
Research Article
Selectivity
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Title Low-Energy Collisions of Protonated Enantiopure Amino Acids with Chiral Target Gases
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Volume 28
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