Evaluation of pyridoindoles, pyridylindoles and pyridylpyridoindoles as matrices for ultraviolet matrix-assisted laser desorption/ionization time-of-flight mass spectrometry

In an effort to gain an understanding of the processes governing ultraviolet matrix-assisted laser desorption/ionization (UV-MALDI), direct comparison was made of the mass spectra of proteins, carbohydrates and synthetic polymers (polyethylene glycol, polyester and polyamide) by using pyridylindoles...

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Autor principal: Erra Balsells, Rosa
Publicado: 2001
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Acceso en línea:https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_09514198_v15_n23_p2354_Nonami
http://hdl.handle.net/20.500.12110/paper_09514198_v15_n23_p2354_Nonami
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spelling paper:paper_09514198_v15_n23_p2354_Nonami2023-06-08T15:54:57Z Evaluation of pyridoindoles, pyridylindoles and pyridylpyridoindoles as matrices for ultraviolet matrix-assisted laser desorption/ionization time-of-flight mass spectrometry Erra Balsells, Rosa 2,5-dihydroxybenzoic acid bipyridine derivative carbohydrate carboline derivative cyclodextrin gentisic acid harman harmine hydrogen hydroxybenzoic acid derivative indole derivative maneb nitrogen polymer protein pyridine derivative pyrifenox mancozeb pyrifenox-mancozeb zineb article carbohydrate analysis chemistry crystallization desorption drug combination ionization mass spectrometry methodology protein analysis protein structure ultraviolet radiation ultraviolet spectrophotometry Carbohydrates Crystallization Drug Combinations Gentisates Harmine Hydroxybenzoic Acids Indoles Maneb Polymers Proteins Pyridines Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization Spectrophotometry, Ultraviolet Zineb In an effort to gain an understanding of the processes governing ultraviolet matrix-assisted laser desorption/ionization (UV-MALDI), direct comparison was made of the mass spectra of proteins, carbohydrates and synthetic polymers (polyethylene glycol, polyester and polyamide) by using pyridylindoles, pyridoindoles and pyridylpyridoindoles as UV (337 nm)-MALDI-TOFMS matrices in positive and negative ion mode. In order to study the combined effect of the indole N-H and the pyridine nitrogen of the MALDI matrix on the desorption/ionization process in MALDI, compounds were selected that include either or both of these functions in their structure. Within the compounds studied only those that possess simultaneously both functions in a 1,4-relation behave as very good matrices for proteins. These compounds also work as matrices for some carbohydrates and synthetic polymers used as analytes in the present study. Some of the compounds were also found to be useful for the post-source decay (PSD) analysis of cyclodextrins in positive and negative ion mode. In several cases we also examined the matrix behavior of the corresponding N-methylindole derivatives. Copyright © 2001 John Wiley & Sons, Ltd. Fil:Erra-Balsells, R. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. 2001 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_09514198_v15_n23_p2354_Nonami http://hdl.handle.net/20.500.12110/paper_09514198_v15_n23_p2354_Nonami
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic 2,5-dihydroxybenzoic acid
bipyridine derivative
carbohydrate
carboline derivative
cyclodextrin
gentisic acid
harman
harmine
hydrogen
hydroxybenzoic acid derivative
indole derivative
maneb
nitrogen
polymer
protein
pyridine derivative
pyrifenox mancozeb
pyrifenox-mancozeb
zineb
article
carbohydrate analysis
chemistry
crystallization
desorption
drug combination
ionization
mass spectrometry
methodology
protein analysis
protein structure
ultraviolet radiation
ultraviolet spectrophotometry
Carbohydrates
Crystallization
Drug Combinations
Gentisates
Harmine
Hydroxybenzoic Acids
Indoles
Maneb
Polymers
Proteins
Pyridines
Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization
Spectrophotometry, Ultraviolet
Zineb
spellingShingle 2,5-dihydroxybenzoic acid
bipyridine derivative
carbohydrate
carboline derivative
cyclodextrin
gentisic acid
harman
harmine
hydrogen
hydroxybenzoic acid derivative
indole derivative
maneb
nitrogen
polymer
protein
pyridine derivative
pyrifenox mancozeb
pyrifenox-mancozeb
zineb
article
carbohydrate analysis
chemistry
crystallization
desorption
drug combination
ionization
mass spectrometry
methodology
protein analysis
protein structure
ultraviolet radiation
ultraviolet spectrophotometry
Carbohydrates
Crystallization
Drug Combinations
Gentisates
Harmine
Hydroxybenzoic Acids
Indoles
Maneb
Polymers
Proteins
Pyridines
Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization
Spectrophotometry, Ultraviolet
Zineb
Erra Balsells, Rosa
Evaluation of pyridoindoles, pyridylindoles and pyridylpyridoindoles as matrices for ultraviolet matrix-assisted laser desorption/ionization time-of-flight mass spectrometry
topic_facet 2,5-dihydroxybenzoic acid
bipyridine derivative
carbohydrate
carboline derivative
cyclodextrin
gentisic acid
harman
harmine
hydrogen
hydroxybenzoic acid derivative
indole derivative
maneb
nitrogen
polymer
protein
pyridine derivative
pyrifenox mancozeb
pyrifenox-mancozeb
zineb
article
carbohydrate analysis
chemistry
crystallization
desorption
drug combination
ionization
mass spectrometry
methodology
protein analysis
protein structure
ultraviolet radiation
ultraviolet spectrophotometry
Carbohydrates
Crystallization
Drug Combinations
Gentisates
Harmine
Hydroxybenzoic Acids
Indoles
Maneb
Polymers
Proteins
Pyridines
Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization
Spectrophotometry, Ultraviolet
Zineb
description In an effort to gain an understanding of the processes governing ultraviolet matrix-assisted laser desorption/ionization (UV-MALDI), direct comparison was made of the mass spectra of proteins, carbohydrates and synthetic polymers (polyethylene glycol, polyester and polyamide) by using pyridylindoles, pyridoindoles and pyridylpyridoindoles as UV (337 nm)-MALDI-TOFMS matrices in positive and negative ion mode. In order to study the combined effect of the indole N-H and the pyridine nitrogen of the MALDI matrix on the desorption/ionization process in MALDI, compounds were selected that include either or both of these functions in their structure. Within the compounds studied only those that possess simultaneously both functions in a 1,4-relation behave as very good matrices for proteins. These compounds also work as matrices for some carbohydrates and synthetic polymers used as analytes in the present study. Some of the compounds were also found to be useful for the post-source decay (PSD) analysis of cyclodextrins in positive and negative ion mode. In several cases we also examined the matrix behavior of the corresponding N-methylindole derivatives. Copyright © 2001 John Wiley & Sons, Ltd.
author Erra Balsells, Rosa
author_facet Erra Balsells, Rosa
author_sort Erra Balsells, Rosa
title Evaluation of pyridoindoles, pyridylindoles and pyridylpyridoindoles as matrices for ultraviolet matrix-assisted laser desorption/ionization time-of-flight mass spectrometry
title_short Evaluation of pyridoindoles, pyridylindoles and pyridylpyridoindoles as matrices for ultraviolet matrix-assisted laser desorption/ionization time-of-flight mass spectrometry
title_full Evaluation of pyridoindoles, pyridylindoles and pyridylpyridoindoles as matrices for ultraviolet matrix-assisted laser desorption/ionization time-of-flight mass spectrometry
title_fullStr Evaluation of pyridoindoles, pyridylindoles and pyridylpyridoindoles as matrices for ultraviolet matrix-assisted laser desorption/ionization time-of-flight mass spectrometry
title_full_unstemmed Evaluation of pyridoindoles, pyridylindoles and pyridylpyridoindoles as matrices for ultraviolet matrix-assisted laser desorption/ionization time-of-flight mass spectrometry
title_sort evaluation of pyridoindoles, pyridylindoles and pyridylpyridoindoles as matrices for ultraviolet matrix-assisted laser desorption/ionization time-of-flight mass spectrometry
publishDate 2001
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_09514198_v15_n23_p2354_Nonami
http://hdl.handle.net/20.500.12110/paper_09514198_v15_n23_p2354_Nonami
work_keys_str_mv AT errabalsellsrosa evaluationofpyridoindolespyridylindolesandpyridylpyridoindolesasmatricesforultravioletmatrixassistedlaserdesorptionionizationtimeofflightmassspectrometry
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