Please use this identifier to cite or link to this item: https://doi.org/10.1038/s41467-018-04461-9
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dc.titleCombining laser capture microdissection and proteomics reveals an active translation machinery controlling invadosome formation
dc.contributor.authorEzzoukhry, Z
dc.contributor.authorHenriet, E
dc.contributor.authorCordelières, F.P
dc.contributor.authorDupuy, J.-W
dc.contributor.authorMaître, M
dc.contributor.authorGay, N
dc.contributor.authorDi-Tommaso, S
dc.contributor.authorMercier, L
dc.contributor.authorGoetz, J.G
dc.contributor.authorPeter, M
dc.contributor.authorBard, F
dc.contributor.authorMoreau, V
dc.contributor.authorRaymond, A.-A
dc.contributor.authorSaltel, F
dc.date.accessioned2020-10-20T09:48:30Z
dc.date.available2020-10-20T09:48:30Z
dc.date.issued2018
dc.identifier.citationEzzoukhry, Z, Henriet, E, Cordelières, F.P, Dupuy, J.-W, Maître, M, Gay, N, Di-Tommaso, S, Mercier, L, Goetz, J.G, Peter, M, Bard, F, Moreau, V, Raymond, A.-A, Saltel, F (2018). Combining laser capture microdissection and proteomics reveals an active translation machinery controlling invadosome formation. Nature Communications 9 (1) : 4461. ScholarBank@NUS Repository. https://doi.org/10.1038/s41467-018-04461-9
dc.identifier.issn2041-1723
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/178410
dc.description.abstractInvadosomes are F-actin-based structures involved in extracellular matrix degradation, cell invasion, and metastasis formation. Analyzing their proteome is crucial to decipher their molecular composition, to understand their mechanisms, and to find specific elements to target them. However, the specific analysis of invadosomes is challenging, because it is difficult to maintain their integrity during isolation. In addition, classical purification methods often suffer from contaminations, which may impair data validation. To ensure the specific identification of invadosome components, we here develop a method that combines laser microdissection and mass spectrometry, enabling the analysis of subcellular structures in their native state based on low amounts of input material. Using this combinatorial method, we show that invadosomes contain specific components of the translational machinery, in addition to known marker proteins. Moreover, functional validation reveals that protein translation activity is an inherent property of invadosomes, which is required to maintain invadosome structure and activity. © 2018 The Author(s).
dc.publisherNature Publishing Group
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceUnpaywall 20201031
dc.subjectbiomarker
dc.subjectlaser method
dc.subjectmachinery
dc.subjectprotein
dc.subjectproteomics
dc.subjectpurification
dc.subjectarticle
dc.subjectcontamination
dc.subjectlaser capture microdissection
dc.subjectmachine
dc.subjectmass spectrometry
dc.subjectpodosome
dc.subjectprotein function
dc.subjectproteomics
dc.subjectstructure activity relation
dc.subjectvalidation process
dc.subjectanimal
dc.subjectextracellular matrix
dc.subjecthigh performance liquid chromatography
dc.subjecthuman
dc.subjectlaser capture microdissection
dc.subjectmetabolism
dc.subjectmouse
dc.subjectneoplasm
dc.subjectNIH 3T3 cell line
dc.subjectpathology
dc.subjectpodosome
dc.subjectprocedures
dc.subjectprotein synthesis
dc.subjectproteomics
dc.subjecttandem mass spectrometry
dc.subjecttumor cell line
dc.subjectactin
dc.subjectmessenger RNA
dc.subjecttumor marker
dc.subjectActins
dc.subjectAnimals
dc.subjectBiomarkers, Tumor
dc.subjectCell Line, Tumor
dc.subjectChromatography, High Pressure Liquid
dc.subjectExtracellular Matrix
dc.subjectHumans
dc.subjectLaser Capture Microdissection
dc.subjectMice
dc.subjectNeoplasms
dc.subjectNIH 3T3 Cells
dc.subjectPodosomes
dc.subjectProtein Biosynthesis
dc.subjectProteomics
dc.subjectRNA, Messenger
dc.subjectTandem Mass Spectrometry
dc.typeArticle
dc.contributor.departmentBIOCHEMISTRY
dc.description.doi10.1038/s41467-018-04461-9
dc.description.sourcetitleNature Communications
dc.description.volume9
dc.description.issue1
dc.description.page4461
dc.published.statepublished
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