Protein identification strategies in MALDI imaging mass spectrometry: a brief review

[Display omitted] Matrix assisted laser desorption/ionization (MALDI) imaging mass spectrometry (IMS) is a powerful technology used to investigate the spatial distributions of thousands of molecules throughout a tissue section from a single experiment. As proteins represent an important group of fun...

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Vydáno v:Current opinion in chemical biology Ročník 48; s. 64 - 72
Hlavní autoři: Ryan, Daniel J, Spraggins, Jeffrey M, Caprioli, Richard M
Médium: Journal Article
Jazyk:angličtina
Vydáno: England Elsevier Ltd 01.02.2019
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ISSN:1367-5931, 1879-0402, 1879-0402
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Abstract [Display omitted] Matrix assisted laser desorption/ionization (MALDI) imaging mass spectrometry (IMS) is a powerful technology used to investigate the spatial distributions of thousands of molecules throughout a tissue section from a single experiment. As proteins represent an important group of functional molecules in tissue and cells, the imaging of proteins has been an important point of focus in the development of IMS technologies and methods. Protein identification is crucial for the biological contextualization of molecular imaging data. However, gas-phase fragmentation efficiency of MALDI generated proteins presents significant challenges, making protein identification directly from tissue difficult. This review highlights methods and technologies specifically related to protein identification that have been developed to overcome these challenges in MALDI IMS experiments.
AbstractList Matrix assisted laser desorption/ionization (MALDI) imaging mass spectrometry (IMS) is a powerful technology used to investigate the spatial distributions of thousands of molecules throughout a tissue section from a single experiment. As proteins represent an important group of functional molecules in tissue and cells, the imaging of proteins has been an important point of focus in the development of IMS technologies and methods. Protein identification is crucial for the biological contextualization of molecular imaging data. However, gas-phase fragmentation efficiency of MALDI generated proteins presents significant challenges, making protein identification directly from tissue difficult. This review highlights methods and technologies specifically related to protein identification that have been developed to overcome these challenges in MALDI IMS experiments.
[Display omitted] Matrix assisted laser desorption/ionization (MALDI) imaging mass spectrometry (IMS) is a powerful technology used to investigate the spatial distributions of thousands of molecules throughout a tissue section from a single experiment. As proteins represent an important group of functional molecules in tissue and cells, the imaging of proteins has been an important point of focus in the development of IMS technologies and methods. Protein identification is crucial for the biological contextualization of molecular imaging data. However, gas-phase fragmentation efficiency of MALDI generated proteins presents significant challenges, making protein identification directly from tissue difficult. This review highlights methods and technologies specifically related to protein identification that have been developed to overcome these challenges in MALDI IMS experiments.
Matrix assisted laser desorption/ionization (MALDI) imaging mass spectrometry (IMS) is a powerful technology used to investigate the spatial distributions of thousands of molecules throughout a tissue section from a single experiment. As proteins represent an important group of functional molecules in tissue and cells, the imaging of proteins has been an important point of focus in the development of IMS technologies and methods. Protein identification is crucial for the biological contextualization of molecular imaging data. However, gas-phase fragmentation efficiency of MALDI generated proteins presents significant challenges, making protein identification directly from tissue difficult. This review highlights methods and technologies specifically related to protein identification that have been developed to overcome these challenges in MALDI IMS experiments.Matrix assisted laser desorption/ionization (MALDI) imaging mass spectrometry (IMS) is a powerful technology used to investigate the spatial distributions of thousands of molecules throughout a tissue section from a single experiment. As proteins represent an important group of functional molecules in tissue and cells, the imaging of proteins has been an important point of focus in the development of IMS technologies and methods. Protein identification is crucial for the biological contextualization of molecular imaging data. However, gas-phase fragmentation efficiency of MALDI generated proteins presents significant challenges, making protein identification directly from tissue difficult. This review highlights methods and technologies specifically related to protein identification that have been developed to overcome these challenges in MALDI IMS experiments.
Author Caprioli, Richard M
Ryan, Daniel J
Spraggins, Jeffrey M
AuthorAffiliation 2 Mass Spectrometry Research Center, Vanderbilt University, 465 21 st Ave S #9160, Nashville, TN 37235, USA
1 Department of Chemistry, Vanderbilt University, 7330 Stevenson Center, Station B 351822, Nashville, TN 37235, USA
4 Department of Pharmacology, Vanderbilt University, 442 Robinson Research Building, 2220 Pierce Avenue, Nashville, TN 37232, USA
3 Department of Biochemistry, Vanderbilt University, 607 Light Hall, Nashville, TN 37205, USA
5 Department of Medicine, Vanderbilt University, 465 21 st Ave #9160, Nashville, TN 37235, USA
AuthorAffiliation_xml – name: 4 Department of Pharmacology, Vanderbilt University, 442 Robinson Research Building, 2220 Pierce Avenue, Nashville, TN 37232, USA
– name: 5 Department of Medicine, Vanderbilt University, 465 21 st Ave #9160, Nashville, TN 37235, USA
– name: 3 Department of Biochemistry, Vanderbilt University, 607 Light Hall, Nashville, TN 37205, USA
– name: 2 Mass Spectrometry Research Center, Vanderbilt University, 465 21 st Ave S #9160, Nashville, TN 37235, USA
– name: 1 Department of Chemistry, Vanderbilt University, 7330 Stevenson Center, Station B 351822, Nashville, TN 37235, USA
Author_xml – sequence: 1
  givenname: Daniel J
  orcidid: 0000-0001-8201-1472
  surname: Ryan
  fullname: Ryan, Daniel J
  organization: Department of Chemistry, Vanderbilt University, 7330 Stevenson Center, Station B 351822, Nashville, TN 37235, USA
– sequence: 2
  givenname: Jeffrey M
  surname: Spraggins
  fullname: Spraggins, Jeffrey M
  organization: Department of Chemistry, Vanderbilt University, 7330 Stevenson Center, Station B 351822, Nashville, TN 37235, USA
– sequence: 3
  givenname: Richard M
  surname: Caprioli
  fullname: Caprioli, Richard M
  email: richard.m.caprioli@Vanderbilt.Edu
  organization: Department of Chemistry, Vanderbilt University, 7330 Stevenson Center, Station B 351822, Nashville, TN 37235, USA
BackLink https://www.ncbi.nlm.nih.gov/pubmed/30476689$$D View this record in MEDLINE/PubMed
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Snippet [Display omitted] Matrix assisted laser desorption/ionization (MALDI) imaging mass spectrometry (IMS) is a powerful technology used to investigate the spatial...
Matrix assisted laser desorption/ionization (MALDI) imaging mass spectrometry (IMS) is a powerful technology used to investigate the spatial distributions of...
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SubjectTerms Animals
Equipment Design
Humans
Molecular Imaging - instrumentation
Molecular Imaging - methods
Proteins - analysis
Proteins - isolation & purification
Specimen Handling - instrumentation
Specimen Handling - methods
Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization - instrumentation
Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization - methods
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Title Protein identification strategies in MALDI imaging mass spectrometry: a brief review
URI https://dx.doi.org/10.1016/j.cbpa.2018.10.023
https://www.ncbi.nlm.nih.gov/pubmed/30476689
https://www.proquest.com/docview/2138646060
https://pubmed.ncbi.nlm.nih.gov/PMC6382520
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