Literature DB >> 27060368

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

Jeffrey M Spraggins1,2,3, David G Rizzo2,3, Jessica L Moore2,3, Michael J Noto4, Eric P Skaar5,6, Richard M Caprioli1,2,3,4,7.   

Abstract

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 μm 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 (∼75 000 at m/z 5000) for proteins up to ∼20 kDa. Analysis of clear cell renal cell carcinoma using MALDI FTICR IMS identified specific proteins localized to healthy tissue regions, within the tumor, and also in areas of increased vascularization around the tumor.
© 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  Cystic fibrosis; FTICR MS; High-throughput; Human clear cell renal cell carcinoma; Nutritional immunity; Technology

Mesh:

Substances:

Year:  2016        PMID: 27060368      PMCID: PMC5117945          DOI: 10.1002/pmic.201600003

Source DB:  PubMed          Journal:  Proteomics        ISSN: 1615-9853            Impact factor:   3.984


  48 in total

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3.  High spatial resolution imaging mass spectrometry and classical histology on a single tissue section.

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Review 5.  Mass spectrometry imaging in drug development.

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6.  High-resolution matrix-assisted laser desorption/ionization imaging of tryptic peptides from tissue.

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7.  Molecular analysis of tumor margins by MALDI mass spectrometry in renal carcinoma.

Authors:  Stacey R Oppenheimer; Deming Mi; Melinda E Sanders; Richard M Caprioli
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8.  Tissue localization and chromosomal assignment of a serum protein that tracks the cystic fibrosis gene.

Authors:  V van Heyningen; C Hayward; J Fletcher; C McAuley
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9.  Tissue protein imaging at 1 μm laser spot diameter for high spatial resolution and high imaging speed using transmission geometry MALDI TOF MS.

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Review 10.  Surgical management of renal cell carcinoma.

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Journal:  Semin Intervent Radiol       Date:  2014-03       Impact factor: 1.513

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  41 in total

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2.  Exosome Isolation by Ultracentrifugation and Precipitation and Techniques for Downstream Analyses.

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3.  Mapping Molecular Datasets Back to the Brain Regions They are Extracted from: Remembering the Native Countries of Hypothalamic Expatriates and Refugees.

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5.  MALDI MS Imaging at Acquisition Rates Exceeding 100 Pixels per Second.

Authors:  Antonín Bednařík; Markéta Machálková; Eugene Moskovets; Kateřina Coufalíková; Pavel Krásenský; Pavel Houška; Jiří Kroupa; Jarmila Navrátilová; Jan Šmarda; Jan Preisler
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6.  Genetically Encoded Fluorescent Proteins Enable High-Throughput Assignment of Cell Cohorts Directly from MALDI-MS Images.

Authors:  Nicholas D Schmitt; Catherine M Rawlins; Elizabeth C Randall; Xianzhe Wang; Antonius Koller; Jared R Auclair; Jane-Marie Kowalski; Paul J Kowalski; Ed Luther; Alexander R Ivanov; Nathalie Y R Agar; Jeffrey N Agar
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Review 7.  Label-free molecular imaging of the kidney.

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8.  Analysis of Chemotherapeutic Drug Delivery at the Single Cell Level Using 3D-MSI-TOF-SIMS.

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10.  Protein identification in imaging mass spectrometry through spatially targeted liquid micro-extractions.

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