The application of innovative spatial proteomics techniques, such as those based upon matrix-assisted laser desorption/ionization mass spectrometry imaging (MALDI-MSI) technology, has the potential to impact research in the field of nephropathology. Notwithstanding, the possibility to apply this technology in more routine diagnostic contexts remains limited by the alternative fixatives employed by this ultraspecialized diagnostic field, where most nephropathology laboratories worldwide use bouin-fixed paraffin-embedded (BFPE) samples. Here, the feasibility of performing MALDI-MSI on BFPE renal tissue is explored, evaluating variability within the trypsin-digested proteome as a result of different preanalytical conditions and comparing them with the more standardized formalin-fixed paraffin-embedded (FFPE) counterparts. A large proportion of the features (270, 68.9%) was detected in both BFPE and FFPE renal samples, demonstrating only limited variability in signal intensity (10.22-10.06%). Samples processed with either fixative were able to discriminate the principal parenchyma regions along with diverse renal substructures, such as glomeruli, tubules, and vessels. This was observed when performing an additional “stress test”, showing comparable results in both BFPE and FFPE samples when the distribution of several amyloid fingerprint proteins was mapped. These results suggest the utility of BFPE tissue specimens in MSI-based nephropathology research, further widening their application in this field.

Bindi, G., Pagani, L., Ceku, J., de Oliveira, G., Porto, N., Monza, N., et al. (2024). Feasibility of MALDI-MSI-Based Proteomics Using Bouin-Fixed Pathology Samples: Untapping the Goldmine of Nephropathology Archives. JOURNAL OF PROTEOME RESEARCH, 23(7 (5 July 2024)), 2542-2551 [10.1021/acs.jproteome.4c00198].

Feasibility of MALDI-MSI-Based Proteomics Using Bouin-Fixed Pathology Samples: Untapping the Goldmine of Nephropathology Archives

Bindi, Greta;Pagani, Lisa;Ceku, Joranda;de Oliveira, Glenda Santos;Porto, Natalia Shelly;Monza, Nicole;Denti, Vanna;Mescia, Federica;Chinello, Clizia;Magni, Fulvio;Pagni, Fabio;L'Imperio, Vincenzo;Smith, Andrew
2024

Abstract

The application of innovative spatial proteomics techniques, such as those based upon matrix-assisted laser desorption/ionization mass spectrometry imaging (MALDI-MSI) technology, has the potential to impact research in the field of nephropathology. Notwithstanding, the possibility to apply this technology in more routine diagnostic contexts remains limited by the alternative fixatives employed by this ultraspecialized diagnostic field, where most nephropathology laboratories worldwide use bouin-fixed paraffin-embedded (BFPE) samples. Here, the feasibility of performing MALDI-MSI on BFPE renal tissue is explored, evaluating variability within the trypsin-digested proteome as a result of different preanalytical conditions and comparing them with the more standardized formalin-fixed paraffin-embedded (FFPE) counterparts. A large proportion of the features (270, 68.9%) was detected in both BFPE and FFPE renal samples, demonstrating only limited variability in signal intensity (10.22-10.06%). Samples processed with either fixative were able to discriminate the principal parenchyma regions along with diverse renal substructures, such as glomeruli, tubules, and vessels. This was observed when performing an additional “stress test”, showing comparable results in both BFPE and FFPE samples when the distribution of several amyloid fingerprint proteins was mapped. These results suggest the utility of BFPE tissue specimens in MSI-based nephropathology research, further widening their application in this field.
Articolo in rivista - Articolo scientifico
amyloidosis; glomerulonephritis; MALDI-MSI; proteomics; renal pathology;
English
13-giu-2024
2024
23
7 (5 July 2024)
2542
2551
none
Bindi, G., Pagani, L., Ceku, J., de Oliveira, G., Porto, N., Monza, N., et al. (2024). Feasibility of MALDI-MSI-Based Proteomics Using Bouin-Fixed Pathology Samples: Untapping the Goldmine of Nephropathology Archives. JOURNAL OF PROTEOME RESEARCH, 23(7 (5 July 2024)), 2542-2551 [10.1021/acs.jproteome.4c00198].
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/10281/485679
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