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A Diazirine‐Modified Membrane Lipid to Study Peptide/Lipid Interactions – Chances and Challenges
Although incorporation of photo‐activatable lipids into membranes potentially opens up novel avenues for investigating interactions with proteins, the question of whether diazirine‐modified lipids are suitable for such studies, remains under debate. Focusing on the potential for studying lipid/pepti...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8597076/ https://www.ncbi.nlm.nih.gov/pubmed/34406694 http://dx.doi.org/10.1002/chem.202102048 |
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author | Dorner, Julia Korn, Patricia Gruhle, Kai Ramsbeck, Daniel Garamus, Vasil M. Lilie, Hauke Meister, Annette Schwieger, Christian Ihling, Christian Sinz, Andrea Drescher, Simon |
author_facet | Dorner, Julia Korn, Patricia Gruhle, Kai Ramsbeck, Daniel Garamus, Vasil M. Lilie, Hauke Meister, Annette Schwieger, Christian Ihling, Christian Sinz, Andrea Drescher, Simon |
author_sort | Dorner, Julia |
collection | PubMed |
description | Although incorporation of photo‐activatable lipids into membranes potentially opens up novel avenues for investigating interactions with proteins, the question of whether diazirine‐modified lipids are suitable for such studies, remains under debate. Focusing on the potential for studying lipid/peptide interactions by cross‐linking mass spectrometry (XL‐MS), we developed a diazirine‐modified lipid (DiazPC), and examined its behaviour in membranes incorporating the model α‐helical peptide LAVA20. We observed an unexpected backfolding of the diazirine‐containing stearoyl chain of the lipid. This surprising behaviour challenges the potential application of DiazPC for future XL‐MS studies of peptide and protein/lipid interactions. The observations made for DiazPC most likely represent a general phenomenon for any type of membrane lipids with a polar moiety incorporated into the alkyl chain. Our finding is therefore of importance for future protein/lipid interaction studies relying on modified lipid probes. |
format | Online Article Text |
id | pubmed-8597076 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-85970762021-11-22 A Diazirine‐Modified Membrane Lipid to Study Peptide/Lipid Interactions – Chances and Challenges Dorner, Julia Korn, Patricia Gruhle, Kai Ramsbeck, Daniel Garamus, Vasil M. Lilie, Hauke Meister, Annette Schwieger, Christian Ihling, Christian Sinz, Andrea Drescher, Simon Chemistry Communications Although incorporation of photo‐activatable lipids into membranes potentially opens up novel avenues for investigating interactions with proteins, the question of whether diazirine‐modified lipids are suitable for such studies, remains under debate. Focusing on the potential for studying lipid/peptide interactions by cross‐linking mass spectrometry (XL‐MS), we developed a diazirine‐modified lipid (DiazPC), and examined its behaviour in membranes incorporating the model α‐helical peptide LAVA20. We observed an unexpected backfolding of the diazirine‐containing stearoyl chain of the lipid. This surprising behaviour challenges the potential application of DiazPC for future XL‐MS studies of peptide and protein/lipid interactions. The observations made for DiazPC most likely represent a general phenomenon for any type of membrane lipids with a polar moiety incorporated into the alkyl chain. Our finding is therefore of importance for future protein/lipid interaction studies relying on modified lipid probes. John Wiley and Sons Inc. 2021-09-28 2021-10-21 /pmc/articles/PMC8597076/ /pubmed/34406694 http://dx.doi.org/10.1002/chem.202102048 Text en © 2021 The Authors. Chemistry - A European Journal published by Wiley-VCH GmbH https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Communications Dorner, Julia Korn, Patricia Gruhle, Kai Ramsbeck, Daniel Garamus, Vasil M. Lilie, Hauke Meister, Annette Schwieger, Christian Ihling, Christian Sinz, Andrea Drescher, Simon A Diazirine‐Modified Membrane Lipid to Study Peptide/Lipid Interactions – Chances and Challenges |
title | A Diazirine‐Modified Membrane Lipid to Study Peptide/Lipid Interactions – Chances and Challenges |
title_full | A Diazirine‐Modified Membrane Lipid to Study Peptide/Lipid Interactions – Chances and Challenges |
title_fullStr | A Diazirine‐Modified Membrane Lipid to Study Peptide/Lipid Interactions – Chances and Challenges |
title_full_unstemmed | A Diazirine‐Modified Membrane Lipid to Study Peptide/Lipid Interactions – Chances and Challenges |
title_short | A Diazirine‐Modified Membrane Lipid to Study Peptide/Lipid Interactions – Chances and Challenges |
title_sort | diazirine‐modified membrane lipid to study peptide/lipid interactions – chances and challenges |
topic | Communications |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8597076/ https://www.ncbi.nlm.nih.gov/pubmed/34406694 http://dx.doi.org/10.1002/chem.202102048 |
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