Next-generation technologies for spatial proteomics: Integrating ultra-high speed MALDI-TOF and high mass resolution MALDI FTICR imaging mass spectrometry for protein analysis

作者：Spraggins Jeffrey M^*; Rizzo David G; Moore Jessica L; Noto Michael J; Skaar Eric P; Caprioli Richard M

来源：Proteomics, 2016, 16(11-12): 1678-1689.

DOI：10.1002/pmic.201600003

• Cystic fibrosis
• FTICR MS
• High-throughput
• Human clear cell renal cell carcinoma
• Nutritional immunity
• Technology

MALDI imaging mass spectrometry is a powerful analytical tool enabling the visualization of biomolecules in tissue. However, there are unique challenges associated with protein imaging experiments including the need for higher spatial resolution capabilities, improved image acquisition rates, and better molecular specificity. Here we demonstrate the capabilities of ultra-high speed MALDI-TOF and high mass resolution MALDI FTICR IMS platforms as they relate to these challenges. High spatial resolution MALDI-TOF protein images of rat brain tissue and cystic fibrosis lung tissue were acquired at image acquisition rates >25 pixels/s. Structures as small as 50 mu m were spatially resolved and proteins associated with host immune response were observed in cystic fibrosis lung tissue. Ultra-high speed MALDI-TOF enables unique applications including megapixel molecular imaging as demonstrated for lipid analysis of cystic fibrosis lung tissue. Additionally, imaging experiments using MALDI FTICR IMS were shown to produce data with high mass accuracy (<5 ppm) and resolving power (similar to 75 000 at m/z 5000) for proteins up to similar to 20 kDa. Analysis of clear cell renal cell carcinoma usingMALDI FTICR IMS identified specific proteins localized to healthy tissue regions, within the tumor, and also in areas of increased vascularization around the tumor.

• 出版日期2016-6