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A lysine-based 2:1-[α/aza]-pseudopeptide series used as additives in polymeric membranes for CO(2) capture: synthesis, structural studies, and application

The current study presents for the first time the synthesis of a new 2:1-[α/aza]-pseudopeptide series possessing charged amino acids (i.e., lysine) and aims at studying the influences of chirality, backbone length, and the nature of the lysine side chains on the conformation of the 2:1-[α/aza]-oligo...

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Autores principales: Ibrahim, Mohamed I. A., Solimando, Xavier, Stefan, Loïc, Pickaert, Guillaume, Babin, Jérôme, Arnal-Herault, Carole, Roizard, Denis, Jonquières, Anne, Bodiguel, Jacques, Averlant-Petit, Marie-Christine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10052764/
https://www.ncbi.nlm.nih.gov/pubmed/37006376
http://dx.doi.org/10.1039/d3ra00409k
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author Ibrahim, Mohamed I. A.
Solimando, Xavier
Stefan, Loïc
Pickaert, Guillaume
Babin, Jérôme
Arnal-Herault, Carole
Roizard, Denis
Jonquières, Anne
Bodiguel, Jacques
Averlant-Petit, Marie-Christine
author_facet Ibrahim, Mohamed I. A.
Solimando, Xavier
Stefan, Loïc
Pickaert, Guillaume
Babin, Jérôme
Arnal-Herault, Carole
Roizard, Denis
Jonquières, Anne
Bodiguel, Jacques
Averlant-Petit, Marie-Christine
author_sort Ibrahim, Mohamed I. A.
collection PubMed
description The current study presents for the first time the synthesis of a new 2:1-[α/aza]-pseudopeptide series possessing charged amino acids (i.e., lysine) and aims at studying the influences of chirality, backbone length, and the nature of the lysine side chains on the conformation of the 2:1-[α/aza]-oligomers in solution using NMR, FTIR spectroscopy and molecular dynamic calculations. The spectroscopic results emphasized the conservation of the β-turn conformation adopted by the trimers regardless of the chirality which demonstrated a noticeable effect on the conformation of homochiral hexamer (8c) compared with the hetero-analogue (8d). The molecular dynamic calculations predicted that the chirality and the side chain of the lysine residues caused a little distortion from the classical β-turn conformation in the case of short trimer sequences (7c and 7d), while the chirality and the backbone length exerted more distortion on the β-turn adopted by the longer hexamer sequences (8c and 8d). The large disturbance in hexamers from classical β-turn was attributed to increasing the flexibility and the possibility of molecules to adopt a more energetically favorable conformation stabilized by non-classical β-turn intramolecular hydrogen bonds. Thus, alternating d- and l-lysine amino acids in the 2:1-[α/aza]-hexamer (8d) decreases the high steric hindrance between the lysine side chains, as in the homo analogue (8c), and the distortion is less recognized. Finally, short sequences of aza-pseudopeptides containing lysine residues improve CO(2) separation when used as additives in Pebax® 1074 membranes. The best membrane performances were obtained with a pseudopeptidic dimer as an additive (6b′; deprotected lysine side chain), with an increase in both ideal selectivity α(CO(2)/N(2)) (from 42.8 to 47.6) and CO(2) permeability (from 132 to 148 Barrer) compared to the virgin Pebax® 1074 membrane.
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spelling pubmed-100527642023-03-30 A lysine-based 2:1-[α/aza]-pseudopeptide series used as additives in polymeric membranes for CO(2) capture: synthesis, structural studies, and application Ibrahim, Mohamed I. A. Solimando, Xavier Stefan, Loïc Pickaert, Guillaume Babin, Jérôme Arnal-Herault, Carole Roizard, Denis Jonquières, Anne Bodiguel, Jacques Averlant-Petit, Marie-Christine RSC Adv Chemistry The current study presents for the first time the synthesis of a new 2:1-[α/aza]-pseudopeptide series possessing charged amino acids (i.e., lysine) and aims at studying the influences of chirality, backbone length, and the nature of the lysine side chains on the conformation of the 2:1-[α/aza]-oligomers in solution using NMR, FTIR spectroscopy and molecular dynamic calculations. The spectroscopic results emphasized the conservation of the β-turn conformation adopted by the trimers regardless of the chirality which demonstrated a noticeable effect on the conformation of homochiral hexamer (8c) compared with the hetero-analogue (8d). The molecular dynamic calculations predicted that the chirality and the side chain of the lysine residues caused a little distortion from the classical β-turn conformation in the case of short trimer sequences (7c and 7d), while the chirality and the backbone length exerted more distortion on the β-turn adopted by the longer hexamer sequences (8c and 8d). The large disturbance in hexamers from classical β-turn was attributed to increasing the flexibility and the possibility of molecules to adopt a more energetically favorable conformation stabilized by non-classical β-turn intramolecular hydrogen bonds. Thus, alternating d- and l-lysine amino acids in the 2:1-[α/aza]-hexamer (8d) decreases the high steric hindrance between the lysine side chains, as in the homo analogue (8c), and the distortion is less recognized. Finally, short sequences of aza-pseudopeptides containing lysine residues improve CO(2) separation when used as additives in Pebax® 1074 membranes. The best membrane performances were obtained with a pseudopeptidic dimer as an additive (6b′; deprotected lysine side chain), with an increase in both ideal selectivity α(CO(2)/N(2)) (from 42.8 to 47.6) and CO(2) permeability (from 132 to 148 Barrer) compared to the virgin Pebax® 1074 membrane. The Royal Society of Chemistry 2023-03-29 /pmc/articles/PMC10052764/ /pubmed/37006376 http://dx.doi.org/10.1039/d3ra00409k Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Ibrahim, Mohamed I. A.
Solimando, Xavier
Stefan, Loïc
Pickaert, Guillaume
Babin, Jérôme
Arnal-Herault, Carole
Roizard, Denis
Jonquières, Anne
Bodiguel, Jacques
Averlant-Petit, Marie-Christine
A lysine-based 2:1-[α/aza]-pseudopeptide series used as additives in polymeric membranes for CO(2) capture: synthesis, structural studies, and application
title A lysine-based 2:1-[α/aza]-pseudopeptide series used as additives in polymeric membranes for CO(2) capture: synthesis, structural studies, and application
title_full A lysine-based 2:1-[α/aza]-pseudopeptide series used as additives in polymeric membranes for CO(2) capture: synthesis, structural studies, and application
title_fullStr A lysine-based 2:1-[α/aza]-pseudopeptide series used as additives in polymeric membranes for CO(2) capture: synthesis, structural studies, and application
title_full_unstemmed A lysine-based 2:1-[α/aza]-pseudopeptide series used as additives in polymeric membranes for CO(2) capture: synthesis, structural studies, and application
title_short A lysine-based 2:1-[α/aza]-pseudopeptide series used as additives in polymeric membranes for CO(2) capture: synthesis, structural studies, and application
title_sort lysine-based 2:1-[α/aza]-pseudopeptide series used as additives in polymeric membranes for co(2) capture: synthesis, structural studies, and application
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10052764/
https://www.ncbi.nlm.nih.gov/pubmed/37006376
http://dx.doi.org/10.1039/d3ra00409k
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