id paper:paper_01666851_v182_n1-2_p88_Pinero
record_format dspace
spelling paper:paper_01666851_v182_n1-2_p88_Pinero2023-06-08T15:16:01Z Metabolic oligosaccharide engineering of Plasmodium falciparum intraerythrocytic stages allows direct glycolipid analysis by mass spectrometry Glycolipids Metabolic oligosaccharide engineering P. falciparum glucosamine derivative glycolipid glycosphingolipid glycosylphosphatidylinositol n azidoglucosamine oligosaccharide unclassified drug article erythrocyte fluorescence analysis glycosylation mass spectrometry matrix assisted laser desorption ionization time of flight mass spectrometry Plasmodium falciparum priority journal structure analysis thin layer chromatography ultraviolet radiation Chromatography, Thin Layer Erythrocytes Fluorescent Dyes Glycolipids Glycosphingolipids Glycosylation Glycosylphosphatidylinositols Mass Spectrometry Metabolic Engineering Oligosaccharides Plasmodium falciparum Staining and Labeling Plasmodium falciparum A recent addition to the arsenal of tools for glycome analysis is the use of metabolic labels that allow covalent tagging of glycans with imaging probes. In this work we show that N-azidoglucosamine was successfully incorporated into glycolipidic structures of Plasmodium falciparum intraerythrocytic stages. The ability to tag glycoconjugates selectively with a fluorescent reporter group permits TLC detection of the glycolipids providing a new method to quantify dynamic changes in the glycosylation pattern and facilitating direct mass spectrometry analyses. Presence of glycosylphosphatidylinositol and glycosphingolipid structures was determined in the different extracts. Furthermore, the fluorescent tag was used as internal matrix for the MALDI experiment making even easier the analysis. © 2012 Elsevier B.V. 2012 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_01666851_v182_n1-2_p88_Pinero http://hdl.handle.net/20.500.12110/paper_01666851_v182_n1-2_p88_Pinero
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic Glycolipids
Metabolic oligosaccharide engineering
P. falciparum
glucosamine derivative
glycolipid
glycosphingolipid
glycosylphosphatidylinositol
n azidoglucosamine
oligosaccharide
unclassified drug
article
erythrocyte
fluorescence analysis
glycosylation
mass spectrometry
matrix assisted laser desorption ionization time of flight mass spectrometry
Plasmodium falciparum
priority journal
structure analysis
thin layer chromatography
ultraviolet radiation
Chromatography, Thin Layer
Erythrocytes
Fluorescent Dyes
Glycolipids
Glycosphingolipids
Glycosylation
Glycosylphosphatidylinositols
Mass Spectrometry
Metabolic Engineering
Oligosaccharides
Plasmodium falciparum
Staining and Labeling
Plasmodium falciparum
spellingShingle Glycolipids
Metabolic oligosaccharide engineering
P. falciparum
glucosamine derivative
glycolipid
glycosphingolipid
glycosylphosphatidylinositol
n azidoglucosamine
oligosaccharide
unclassified drug
article
erythrocyte
fluorescence analysis
glycosylation
mass spectrometry
matrix assisted laser desorption ionization time of flight mass spectrometry
Plasmodium falciparum
priority journal
structure analysis
thin layer chromatography
ultraviolet radiation
Chromatography, Thin Layer
Erythrocytes
Fluorescent Dyes
Glycolipids
Glycosphingolipids
Glycosylation
Glycosylphosphatidylinositols
Mass Spectrometry
Metabolic Engineering
Oligosaccharides
Plasmodium falciparum
Staining and Labeling
Plasmodium falciparum
Metabolic oligosaccharide engineering of Plasmodium falciparum intraerythrocytic stages allows direct glycolipid analysis by mass spectrometry
topic_facet Glycolipids
Metabolic oligosaccharide engineering
P. falciparum
glucosamine derivative
glycolipid
glycosphingolipid
glycosylphosphatidylinositol
n azidoglucosamine
oligosaccharide
unclassified drug
article
erythrocyte
fluorescence analysis
glycosylation
mass spectrometry
matrix assisted laser desorption ionization time of flight mass spectrometry
Plasmodium falciparum
priority journal
structure analysis
thin layer chromatography
ultraviolet radiation
Chromatography, Thin Layer
Erythrocytes
Fluorescent Dyes
Glycolipids
Glycosphingolipids
Glycosylation
Glycosylphosphatidylinositols
Mass Spectrometry
Metabolic Engineering
Oligosaccharides
Plasmodium falciparum
Staining and Labeling
Plasmodium falciparum
description A recent addition to the arsenal of tools for glycome analysis is the use of metabolic labels that allow covalent tagging of glycans with imaging probes. In this work we show that N-azidoglucosamine was successfully incorporated into glycolipidic structures of Plasmodium falciparum intraerythrocytic stages. The ability to tag glycoconjugates selectively with a fluorescent reporter group permits TLC detection of the glycolipids providing a new method to quantify dynamic changes in the glycosylation pattern and facilitating direct mass spectrometry analyses. Presence of glycosylphosphatidylinositol and glycosphingolipid structures was determined in the different extracts. Furthermore, the fluorescent tag was used as internal matrix for the MALDI experiment making even easier the analysis. © 2012 Elsevier B.V.
title Metabolic oligosaccharide engineering of Plasmodium falciparum intraerythrocytic stages allows direct glycolipid analysis by mass spectrometry
title_short Metabolic oligosaccharide engineering of Plasmodium falciparum intraerythrocytic stages allows direct glycolipid analysis by mass spectrometry
title_full Metabolic oligosaccharide engineering of Plasmodium falciparum intraerythrocytic stages allows direct glycolipid analysis by mass spectrometry
title_fullStr Metabolic oligosaccharide engineering of Plasmodium falciparum intraerythrocytic stages allows direct glycolipid analysis by mass spectrometry
title_full_unstemmed Metabolic oligosaccharide engineering of Plasmodium falciparum intraerythrocytic stages allows direct glycolipid analysis by mass spectrometry
title_sort metabolic oligosaccharide engineering of plasmodium falciparum intraerythrocytic stages allows direct glycolipid analysis by mass spectrometry
publishDate 2012
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_01666851_v182_n1-2_p88_Pinero
http://hdl.handle.net/20.500.12110/paper_01666851_v182_n1-2_p88_Pinero
_version_ 1768546154994204672