Spatial distribution of trace metals and associated transport proteins during bacterial infection.
- Publisher:
- Springer
- Publication Type:
- Journal Article
- Citation:
- Analytical and Bioanalytical Chemistry, 2024, 416, (11), pp. 2783-2796
- Issue Date:
- 2024-12-07
Closed Access
Filename | Description | Size | |||
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s00216-023-05068-w.pdf | Published version | 2.94 MB |
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Full metadata record
Field | Value | Language |
---|---|---|
dc.contributor.author | Gonzalez de Vega, R | |
dc.contributor.author | Clases, D | |
dc.contributor.author | Cunningham, BA | |
dc.contributor.author | Ganio, K | |
dc.contributor.author | Neville, SL | |
dc.contributor.author | McDevitt, CA | |
dc.contributor.author | Doble, PA | |
dc.date.accessioned | 2025-01-22T04:31:04Z | |
dc.date.available | 2023-11-20 | |
dc.date.available | 2025-01-22T04:31:04Z | |
dc.date.issued | 2024-12-07 | |
dc.identifier.citation | Analytical and Bioanalytical Chemistry, 2024, 416, (11), pp. 2783-2796 | |
dc.identifier.issn | 1618-2642 | |
dc.identifier.issn | 1618-2650 | |
dc.identifier.uri | http://hdl.handle.net/10453/183997 | |
dc.description.abstract | Innate immune systems alter the concentrations of trace elements in host niches in response to invading pathogens during infection. This work reports the interplay between d-block metal ions and their associated biomolecules using hyphenated elemental techniques to spatially quantify both elemental distributions and the abundance of specific transport proteins. Here, lung tissues were collected for analyses from naïve and Streptococcus pneumoniae-infected mice fed on a zinc-restricted or zinc-supplemented diet. Spatiotemporal distributions of manganese (55Mn), iron (56Fe), copper (63Cu), and zinc (66Zn) were determined by quantitative laser ablation-inductively coupled plasma-mass spectrometry. The murine transport proteins ZIP8 and ZIP14, which are associated with zinc transport, were also imaged by incorporation of immunohistochemistry techniques into the analytical workflow. Collectively, this work demonstrates the potential of a single instrumental platform suitable for multiplex analyses of tissues and labelled antibodies to investigate complex elemental interactions at the host-pathogen interface. Further, these methods have the potential for broad application to investigations of biological pathways where concomitant measurement of elements and biomolecules is crucial to understand the basis of disease and aid in development of new therapeutic approaches. | |
dc.format | Print-Electronic | |
dc.language | eng | |
dc.publisher | Springer | |
dc.relation | http://purl.org/au-research/grants/arc/DP190102361 | |
dc.relation.ispartof | Analytical and Bioanalytical Chemistry | |
dc.relation.isbasedon | 10.1007/s00216-023-05068-w | |
dc.rights | info:eu-repo/semantics/closedAccess | |
dc.subject | 03 Chemical Sciences, 06 Biological Sciences, 09 Engineering | |
dc.subject.classification | Analytical Chemistry | |
dc.subject.classification | 31 Biological sciences | |
dc.subject.classification | 34 Chemical sciences | |
dc.subject.classification | 40 Engineering | |
dc.subject.mesh | Mice | |
dc.subject.mesh | Animals | |
dc.subject.mesh | Carrier Proteins | |
dc.subject.mesh | Mass Spectrometry | |
dc.subject.mesh | Trace Elements | |
dc.subject.mesh | Zinc | |
dc.subject.mesh | Copper | |
dc.subject.mesh | Bacterial Infections | |
dc.subject.mesh | Animals | |
dc.subject.mesh | Mice | |
dc.subject.mesh | Bacterial Infections | |
dc.subject.mesh | Copper | |
dc.subject.mesh | Zinc | |
dc.subject.mesh | Trace Elements | |
dc.subject.mesh | Carrier Proteins | |
dc.subject.mesh | Mass Spectrometry | |
dc.subject.mesh | Mice | |
dc.subject.mesh | Animals | |
dc.subject.mesh | Carrier Proteins | |
dc.subject.mesh | Mass Spectrometry | |
dc.subject.mesh | Trace Elements | |
dc.subject.mesh | Zinc | |
dc.subject.mesh | Copper | |
dc.subject.mesh | Bacterial Infections | |
dc.title | Spatial distribution of trace metals and associated transport proteins during bacterial infection. | |
dc.type | Journal Article | |
utslib.citation.volume | 416 | |
utslib.location.activity | Germany | |
utslib.for | 03 Chemical Sciences | |
utslib.for | 06 Biological Sciences | |
utslib.for | 09 Engineering | |
pubs.organisational-group | University of Technology Sydney | |
pubs.organisational-group | University of Technology Sydney/Faculty of Science | |
pubs.organisational-group | University of Technology Sydney/Faculty of Science/School of Mathematical and Physical Sciences | |
utslib.copyright.status | closed_access | * |
pubs.consider-herdc | false | |
dc.date.updated | 2025-01-22T04:31:02Z | |
pubs.issue | 11 | |
pubs.publication-status | Published online | |
pubs.volume | 416 | |
utslib.citation.issue | 11 |
Abstract:
Innate immune systems alter the concentrations of trace elements in host niches in response to invading pathogens during infection. This work reports the interplay between d-block metal ions and their associated biomolecules using hyphenated elemental techniques to spatially quantify both elemental distributions and the abundance of specific transport proteins. Here, lung tissues were collected for analyses from naïve and Streptococcus pneumoniae-infected mice fed on a zinc-restricted or zinc-supplemented diet. Spatiotemporal distributions of manganese (55Mn), iron (56Fe), copper (63Cu), and zinc (66Zn) were determined by quantitative laser ablation-inductively coupled plasma-mass spectrometry. The murine transport proteins ZIP8 and ZIP14, which are associated with zinc transport, were also imaged by incorporation of immunohistochemistry techniques into the analytical workflow. Collectively, this work demonstrates the potential of a single instrumental platform suitable for multiplex analyses of tissues and labelled antibodies to investigate complex elemental interactions at the host-pathogen interface. Further, these methods have the potential for broad application to investigations of biological pathways where concomitant measurement of elements and biomolecules is crucial to understand the basis of disease and aid in development of new therapeutic approaches.
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