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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...

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Autores principales: Warren, Matthew T., Galpin, Iain, Bachtiger, Fabienne, Gibson, Matthew I., Sosso, Gabriele C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2022
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.
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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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