Micro-Sampling of Biological Tissue by ...
Type de document :
Autre communication scientifique (congrès sans actes - poster - séminaire...)
Titre :
Micro-Sampling of Biological Tissue by Substrate-Mediated Laser Ablation: Toward Spatially-Resolved Proteomics at µm Scale
Auteur(s) :
Maulouet, T [Auteur]
Fatou, B [Auteur]
Salzet, M. [Auteur]
Neuroimmunologie des annélides [NA]
Fournier, Isabelle [Auteur]
Neuroimmunologie des annélides [NA]
Focsa, Cristian [Auteur]
Laboratoire de Physique des Lasers, Atomes et Molécules - UMR 8523 [PhLAM]
Ziskind, Michael [Auteur]
Laboratoire de Physique des Lasers, Atomes et Molécules - UMR 8523 [PhLAM]
Fatou, B [Auteur]
Salzet, M. [Auteur]
Neuroimmunologie des annélides [NA]
Fournier, Isabelle [Auteur]
Neuroimmunologie des annélides [NA]
Focsa, Cristian [Auteur]
Laboratoire de Physique des Lasers, Atomes et Molécules - UMR 8523 [PhLAM]
Ziskind, Michael [Auteur]
Laboratoire de Physique des Lasers, Atomes et Molécules - UMR 8523 [PhLAM]
Titre de la manifestation scientifique :
15th International Conference on Laser Ablation
Ville :
Maui
Pays :
Etats-Unis d'Amérique
Date de début de la manifestation scientifique :
2019-09-08
Discipline(s) HAL :
Sciences du Vivant [q-bio]/Ingénierie biomédicale/Imagerie
Physique [physics]/Physique [physics]/Optique [physics.optics]
Physique [physics]/Physique [physics]/Optique [physics.optics]
Résumé en anglais : [en]
Since the pioneering works of R. Caprioli in 1997, conventional mass spectrometry imaging (MSI) tools resultingfrom Matrix-Assisted Laser Desorption/Ionization (MALDI) is widely used in various fields of -omics research ...
Lire la suite >Since the pioneering works of R. Caprioli in 1997, conventional mass spectrometry imaging (MSI) tools resultingfrom Matrix-Assisted Laser Desorption/Ionization (MALDI) is widely used in various fields of -omics research (e.g.lipidomics, proteomics, metabolomics...) because of its high spatial resolution and detection sensitivity. However, dueto the inherent complexity of the biological tissue it has certain limitations. One of the major drawbacks of thetechnique is the limited capability of detecting and identifying minority compounds, notably proteins, directly ontissue. Various strategies have been developed to overcome this issue. All require a micro-sampling step. Differenttechniques have been specifically applied for this purpose like laser capture microdissection, liquid extraction orparafilm assisted microdissection (PAM) [1]. However, the spatial resolution of these techniques is typically about1mm and it is a real challenge to develop a tool with a sufficient yield to reduce the size of the sampled area.We have explored the potential of a new micro-sampling technique based on an indirect substrate-mediated laserablation (SMLA) mechanism which permits the use of low deposited energy while preserving the biological content.Taking advantage of this effect, analyses of micro-sampled tissue was performed, demonstrating the identification ofsignificant number of proteins [2]. Furthermore, SMLA was confronted to PAM in order to show its efficiency. Ourobjective is now to increase the spatial resolution up to µm scale. This requires the characterization of the SMLAmechanism to optimize the ablation yields. We present here recent advances in this field including systematic studiestaking into account the physico-chemical parameters of various substrates who highlights the role of the ablation ofthe substrate in the SMLA mechanism [3] and the study of the plume dynamic by shadowgraphy used to improve thecapture yield of the ablated material.Lire moins >
Lire la suite >Since the pioneering works of R. Caprioli in 1997, conventional mass spectrometry imaging (MSI) tools resultingfrom Matrix-Assisted Laser Desorption/Ionization (MALDI) is widely used in various fields of -omics research (e.g.lipidomics, proteomics, metabolomics...) because of its high spatial resolution and detection sensitivity. However, dueto the inherent complexity of the biological tissue it has certain limitations. One of the major drawbacks of thetechnique is the limited capability of detecting and identifying minority compounds, notably proteins, directly ontissue. Various strategies have been developed to overcome this issue. All require a micro-sampling step. Differenttechniques have been specifically applied for this purpose like laser capture microdissection, liquid extraction orparafilm assisted microdissection (PAM) [1]. However, the spatial resolution of these techniques is typically about1mm and it is a real challenge to develop a tool with a sufficient yield to reduce the size of the sampled area.We have explored the potential of a new micro-sampling technique based on an indirect substrate-mediated laserablation (SMLA) mechanism which permits the use of low deposited energy while preserving the biological content.Taking advantage of this effect, analyses of micro-sampled tissue was performed, demonstrating the identification ofsignificant number of proteins [2]. Furthermore, SMLA was confronted to PAM in order to show its efficiency. Ourobjective is now to increase the spatial resolution up to µm scale. This requires the characterization of the SMLAmechanism to optimize the ablation yields. We present here recent advances in this field including systematic studiestaking into account the physico-chemical parameters of various substrates who highlights the role of the ablation ofthe substrate in the SMLA mechanism [3] and the study of the plume dynamic by shadowgraphy used to improve thecapture yield of the ablated material.Lire moins >
Langue :
Anglais
Comité de lecture :
Oui
Audience :
Internationale
Vulgarisation :
Non
Source :