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Protein–lipid Association in Lizard Chemical Signals
Chemical communication in terrestrial vertebrates is often built on complex blends, where semiochemical and structural compounds may form an integrated functional unit. In lizards, many species have specialized epidermal glands whose secretions are waxy, homogeneous blends of lipids and proteins, bo...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10205002/ https://www.ncbi.nlm.nih.gov/pubmed/37228571 http://dx.doi.org/10.1093/iob/obad016 |
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author | Mangiacotti, M Baeckens, S Fumagalli, M Martín, J Scali, S Sacchi, R |
author_facet | Mangiacotti, M Baeckens, S Fumagalli, M Martín, J Scali, S Sacchi, R |
author_sort | Mangiacotti, M |
collection | PubMed |
description | Chemical communication in terrestrial vertebrates is often built on complex blends, where semiochemical and structural compounds may form an integrated functional unit. In lizards, many species have specialized epidermal glands whose secretions are waxy, homogeneous blends of lipids and proteins, both active in communication. The intimate co-occurrence of such compounds allows us to hypothesize that they should undergo a certain degree of covariation, considering both their semiochemical role and the support-to-lipid function hypothesized for the protein fraction. In order to assess the occurrence and level of protein–lipid covariation, we compared the composition and complexity of the two fractions in the femoral gland secretions of 36 lizard species, combining phylogenetically-informed analysis with tandem mass spectrometry. We found the composition and complexity of the two fractions to be strongly correlated. The composition of the protein fraction was mostly influenced by the relative proportion of cholestanol, provitamin D(3), stigmasterol, and tocopherol, while the complexity of the protein pattern increased with that of lipids. Additionally, two identified proteins (carbonic anhydrase and protein disulfide isomerase) increased their concentration as provitamin D(3) became more abundant. Although our approach does not allow us to decrypt the functional relations between the proteinaceous and lipid components, nor under the semiochemical or structural hypothesis, the finding that the proteins involved in this association were enzymes opens up to new perspectives about protein role: They may confer dynamic properties to the blend, making it able to compensate predictable variation of the environmental conditions. This may expand the view about proteins in the support-to-lipid hypothesis, from being a passive and inert component of the secretions to become an active and dynamic one, thus providing cues for future research. |
format | Online Article Text |
id | pubmed-10205002 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-102050022023-05-24 Protein–lipid Association in Lizard Chemical Signals Mangiacotti, M Baeckens, S Fumagalli, M Martín, J Scali, S Sacchi, R Integr Org Biol Article Chemical communication in terrestrial vertebrates is often built on complex blends, where semiochemical and structural compounds may form an integrated functional unit. In lizards, many species have specialized epidermal glands whose secretions are waxy, homogeneous blends of lipids and proteins, both active in communication. The intimate co-occurrence of such compounds allows us to hypothesize that they should undergo a certain degree of covariation, considering both their semiochemical role and the support-to-lipid function hypothesized for the protein fraction. In order to assess the occurrence and level of protein–lipid covariation, we compared the composition and complexity of the two fractions in the femoral gland secretions of 36 lizard species, combining phylogenetically-informed analysis with tandem mass spectrometry. We found the composition and complexity of the two fractions to be strongly correlated. The composition of the protein fraction was mostly influenced by the relative proportion of cholestanol, provitamin D(3), stigmasterol, and tocopherol, while the complexity of the protein pattern increased with that of lipids. Additionally, two identified proteins (carbonic anhydrase and protein disulfide isomerase) increased their concentration as provitamin D(3) became more abundant. Although our approach does not allow us to decrypt the functional relations between the proteinaceous and lipid components, nor under the semiochemical or structural hypothesis, the finding that the proteins involved in this association were enzymes opens up to new perspectives about protein role: They may confer dynamic properties to the blend, making it able to compensate predictable variation of the environmental conditions. This may expand the view about proteins in the support-to-lipid hypothesis, from being a passive and inert component of the secretions to become an active and dynamic one, thus providing cues for future research. Oxford University Press 2023-05-08 /pmc/articles/PMC10205002/ /pubmed/37228571 http://dx.doi.org/10.1093/iob/obad016 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of the Society for Integrative and Comparative Biology. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Article Mangiacotti, M Baeckens, S Fumagalli, M Martín, J Scali, S Sacchi, R Protein–lipid Association in Lizard Chemical Signals |
title | Protein–lipid Association in Lizard Chemical Signals |
title_full | Protein–lipid Association in Lizard Chemical Signals |
title_fullStr | Protein–lipid Association in Lizard Chemical Signals |
title_full_unstemmed | Protein–lipid Association in Lizard Chemical Signals |
title_short | Protein–lipid Association in Lizard Chemical Signals |
title_sort | protein–lipid association in lizard chemical signals |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10205002/ https://www.ncbi.nlm.nih.gov/pubmed/37228571 http://dx.doi.org/10.1093/iob/obad016 |
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