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Ice Recrystallization Inhibition by Amino Acids: The Curious Case of Alpha- and Beta-Alanine
[Image: see text] Extremophiles produce macromolecules which inhibit ice recrystallization, but there is increasing interest in discovering and developing small molecules that can modulate ice growth. Realizing their potential requires an understanding of how these molecules function at the atomisti...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9007522/ https://www.ncbi.nlm.nih.gov/pubmed/35238571 http://dx.doi.org/10.1021/acs.jpclett.1c04080 |
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author | Warren, Matthew T. Galpin, Iain Bachtiger, Fabienne Gibson, Matthew I. Sosso, Gabriele C. |
author_facet | Warren, Matthew T. Galpin, Iain Bachtiger, Fabienne Gibson, Matthew I. Sosso, Gabriele C. |
author_sort | Warren, Matthew T. |
collection | PubMed |
description | [Image: see text] Extremophiles produce macromolecules which inhibit ice recrystallization, but there is increasing interest in discovering and developing small molecules that can modulate ice growth. Realizing their potential requires an understanding of how these molecules function at the atomistic level. Here, we report the discovery that the amino acid l-α-alanine demonstrates ice recrystallization inhibition (IRI) activity, functioning at 100 mM (∼10 mg/mL). We combined experimental assays with molecular simulations to investigate this IRI agent, drawing comparison to β-alanine, an isomer of l-α-alanine which displays no IRI activity. We found that the difference in the IRI activity of these molecules does not originate from their ice binding affinity, but from their capacity to (not) become overgrown, dictated by the degree of structural (in)compatibility within the growing ice lattice. These findings shed new light on the microscopic mechanisms of small molecule cryoprotectants, particularly in terms of their molecular structure and overgrowth by ice. |
format | Online Article Text |
id | pubmed-9007522 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-90075222022-04-14 Ice Recrystallization Inhibition by Amino Acids: The Curious Case of Alpha- and Beta-Alanine Warren, Matthew T. Galpin, Iain Bachtiger, Fabienne Gibson, Matthew I. Sosso, Gabriele C. J Phys Chem Lett [Image: see text] Extremophiles produce macromolecules which inhibit ice recrystallization, but there is increasing interest in discovering and developing small molecules that can modulate ice growth. Realizing their potential requires an understanding of how these molecules function at the atomistic level. Here, we report the discovery that the amino acid l-α-alanine demonstrates ice recrystallization inhibition (IRI) activity, functioning at 100 mM (∼10 mg/mL). We combined experimental assays with molecular simulations to investigate this IRI agent, drawing comparison to β-alanine, an isomer of l-α-alanine which displays no IRI activity. We found that the difference in the IRI activity of these molecules does not originate from their ice binding affinity, but from their capacity to (not) become overgrown, dictated by the degree of structural (in)compatibility within the growing ice lattice. These findings shed new light on the microscopic mechanisms of small molecule cryoprotectants, particularly in terms of their molecular structure and overgrowth by ice. American Chemical Society 2022-03-03 2022-03-10 /pmc/articles/PMC9007522/ /pubmed/35238571 http://dx.doi.org/10.1021/acs.jpclett.1c04080 Text en © 2022 American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Warren, Matthew T. Galpin, Iain Bachtiger, Fabienne Gibson, Matthew I. Sosso, Gabriele C. Ice Recrystallization Inhibition by Amino Acids: The Curious Case of Alpha- and Beta-Alanine |
title | Ice Recrystallization Inhibition by Amino Acids: The
Curious Case of Alpha- and Beta-Alanine |
title_full | Ice Recrystallization Inhibition by Amino Acids: The
Curious Case of Alpha- and Beta-Alanine |
title_fullStr | Ice Recrystallization Inhibition by Amino Acids: The
Curious Case of Alpha- and Beta-Alanine |
title_full_unstemmed | Ice Recrystallization Inhibition by Amino Acids: The
Curious Case of Alpha- and Beta-Alanine |
title_short | Ice Recrystallization Inhibition by Amino Acids: The
Curious Case of Alpha- and Beta-Alanine |
title_sort | ice recrystallization inhibition by amino acids: the
curious case of alpha- and beta-alanine |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9007522/ https://www.ncbi.nlm.nih.gov/pubmed/35238571 http://dx.doi.org/10.1021/acs.jpclett.1c04080 |
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