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 in | Journal of the American Society for Mass Spectrometry Vol. 28; no. 12; pp. 2686 - 2691 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
New York
Springer US
01.12.2017
Springer Nature B.V |
Subjects | |
Online Access | Get full text |
ISSN | 1044-0305 1879-1123 1879-1123 |
DOI | 10.1007/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. |
Author_xml | – sequence: 1 givenname: K. orcidid: 0000-0002-6770-1595 surname: Kulyk fullname: Kulyk, K. email: kskulyk@gmail.com organization: Department of Physics, Stockholm University, SCA R&D Centre – sequence: 2 givenname: O. surname: Rebrov fullname: Rebrov, O. organization: Department of Physics, Stockholm University – sequence: 3 givenname: M. surname: Ryding fullname: Ryding, M. organization: Department of Chemistry, University of Oslo – sequence: 4 givenname: R. D. surname: Thomas fullname: Thomas, R. D. organization: Department of Physics, Stockholm University – sequence: 5 givenname: E. surname: Uggerud fullname: Uggerud, E. organization: Department of Chemistry, University of Oslo – sequence: 6 givenname: M. surname: Larsson fullname: Larsson, M. organization: Department of Physics, Stockholm University |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/28936701$$D View this record in MEDLINE/PubMed https://urn.kb.se/resolve?urn=urn:nbn:se:su:diva-150878$$DView record from Swedish Publication Index |
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Keywords | Gas-phase complexes Collision induced dissociation Enantiopure amino acids Chiral target gases Chirality Low-energy collisions |
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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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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 |
URI | https://link.springer.com/article/10.1007/s13361-017-1796-7 https://www.ncbi.nlm.nih.gov/pubmed/28936701 https://www.proquest.com/docview/1970202594 https://www.proquest.com/docview/1942673608 https://pubmed.ncbi.nlm.nih.gov/PMC5707228 https://urn.kb.se/resolve?urn=urn:nbn:se:su:diva-150878 |
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