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LILBID-MS: using lasers to shed light on biomolecular architectures

Structural Biology has moved beyond the aim of simply identifying the components of a cellular subsystem towards analysing the dynamics and interactions of multiple players within a cell. This focal shift comes with additional requirements for the analytical tools used to investigate these systems o...

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Detalles Bibliográficos
Autores principales: Hellwig, Nils, Martin, Janosch, Morgner, Nina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Portland Press Ltd. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9317959/
https://www.ncbi.nlm.nih.gov/pubmed/35695670
http://dx.doi.org/10.1042/BST20190881
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author Hellwig, Nils
Martin, Janosch
Morgner, Nina
author_facet Hellwig, Nils
Martin, Janosch
Morgner, Nina
author_sort Hellwig, Nils
collection PubMed
description Structural Biology has moved beyond the aim of simply identifying the components of a cellular subsystem towards analysing the dynamics and interactions of multiple players within a cell. This focal shift comes with additional requirements for the analytical tools used to investigate these systems of increased size and complexity, such as Native Mass Spectrometry, which has always been an important tool for structural biology. Scientific advance and recent developments, such as new ways to mimic a cell membrane for a membrane protein, have caused established methods to struggle to keep up with the increased demands. In this review, we summarize the possibilities, which Laser Induced Liquid Bead Ion Desorption (LILBID) mass spectrometry offers with regard to the challenges of modern structural biology, like increasingly complex sample composition, novel membrane mimics and advanced structural analysis, including next neighbor relations and the dynamics of complex formation.
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spelling pubmed-93179592022-08-05 LILBID-MS: using lasers to shed light on biomolecular architectures Hellwig, Nils Martin, Janosch Morgner, Nina Biochem Soc Trans Review Articles Structural Biology has moved beyond the aim of simply identifying the components of a cellular subsystem towards analysing the dynamics and interactions of multiple players within a cell. This focal shift comes with additional requirements for the analytical tools used to investigate these systems of increased size and complexity, such as Native Mass Spectrometry, which has always been an important tool for structural biology. Scientific advance and recent developments, such as new ways to mimic a cell membrane for a membrane protein, have caused established methods to struggle to keep up with the increased demands. In this review, we summarize the possibilities, which Laser Induced Liquid Bead Ion Desorption (LILBID) mass spectrometry offers with regard to the challenges of modern structural biology, like increasingly complex sample composition, novel membrane mimics and advanced structural analysis, including next neighbor relations and the dynamics of complex formation. Portland Press Ltd. 2022-06-30 2022-06-13 /pmc/articles/PMC9317959/ /pubmed/35695670 http://dx.doi.org/10.1042/BST20190881 Text en © 2022 The Author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article published by Portland Press Limited on behalf of the Biochemical Society and distributed under the Creative Commons Attribution License 4.0 (CC BY) (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Review Articles
Hellwig, Nils
Martin, Janosch
Morgner, Nina
LILBID-MS: using lasers to shed light on biomolecular architectures
title LILBID-MS: using lasers to shed light on biomolecular architectures
title_full LILBID-MS: using lasers to shed light on biomolecular architectures
title_fullStr LILBID-MS: using lasers to shed light on biomolecular architectures
title_full_unstemmed LILBID-MS: using lasers to shed light on biomolecular architectures
title_short LILBID-MS: using lasers to shed light on biomolecular architectures
title_sort lilbid-ms: using lasers to shed light on biomolecular architectures
topic Review Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9317959/
https://www.ncbi.nlm.nih.gov/pubmed/35695670
http://dx.doi.org/10.1042/BST20190881
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