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High Throughput ELISAs to Measure a Unique Glycan on Transferrin in Cerebrospinal Fluid: A Possible Extension toward Alzheimer's Disease Biomarker Development

We have established high-throughput lectin-antibody ELISAs to measure different glycans on transferrin (Tf) in cerebrospinal fluid (CSF) using lectins and an anti-transferrin antibody (TfAb). Lectin blot and precipitation analysis of CSF revealed that PVL (Psathyrella velutina lectin) bound an uniqu...

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Autores principales: Shirotani, Keiro, Futakawa, Satoshi, Nara, Kiyomitsu, Hoshi, Kyoka, Saito, Toshie, Tohyama, Yuriko, Kitazume, Shinobu, Yuasa, Tatsuhiko, Miyajima, Masakazu, Arai, Hajime, Kuno, Atsushi, Narimatsu, Hisashi, Hashimoto, Yasuhiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE-Hindawi Access to Research 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3160710/
https://www.ncbi.nlm.nih.gov/pubmed/21876827
http://dx.doi.org/10.4061/2011/352787
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author Shirotani, Keiro
Futakawa, Satoshi
Nara, Kiyomitsu
Hoshi, Kyoka
Saito, Toshie
Tohyama, Yuriko
Kitazume, Shinobu
Yuasa, Tatsuhiko
Miyajima, Masakazu
Arai, Hajime
Kuno, Atsushi
Narimatsu, Hisashi
Hashimoto, Yasuhiro
author_facet Shirotani, Keiro
Futakawa, Satoshi
Nara, Kiyomitsu
Hoshi, Kyoka
Saito, Toshie
Tohyama, Yuriko
Kitazume, Shinobu
Yuasa, Tatsuhiko
Miyajima, Masakazu
Arai, Hajime
Kuno, Atsushi
Narimatsu, Hisashi
Hashimoto, Yasuhiro
author_sort Shirotani, Keiro
collection PubMed
description We have established high-throughput lectin-antibody ELISAs to measure different glycans on transferrin (Tf) in cerebrospinal fluid (CSF) using lectins and an anti-transferrin antibody (TfAb). Lectin blot and precipitation analysis of CSF revealed that PVL (Psathyrella velutina lectin) bound an unique N-acetylglucosamine-terminated N-glycans on “CSF-type” Tf whereas SSA (Sambucus sieboldiana agglutinin) bound α2,6-N-acetylneuraminic acid-terminated N-glycans on “serum-type” Tf. PVL-TfAb ELISA of 0.5 μL CSF samples detected “CSF-type” Tf but not “serum-type” Tf whereas SSA-TfAb ELISA detected “serum-type” Tf but not “CSF-type” Tf, demonstrating the specificity of the lectin-TfAb ELISAs. In idiopathic normal pressure hydrocephalus (iNPH), a senile dementia associated with ventriculomegaly, amounts of the SSA-reactive Tf were significantly higher than in non-iNPH patients, indicating that Tf glycan analysis by the high-throughput lectin-TfAb ELISAs could become practical diagnostic tools for iNPH. The lectin-antibody ELISAs of CSF proteins might be useful for diagnosis of the other neurological diseases.
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spelling pubmed-31607102011-08-29 High Throughput ELISAs to Measure a Unique Glycan on Transferrin in Cerebrospinal Fluid: A Possible Extension toward Alzheimer's Disease Biomarker Development Shirotani, Keiro Futakawa, Satoshi Nara, Kiyomitsu Hoshi, Kyoka Saito, Toshie Tohyama, Yuriko Kitazume, Shinobu Yuasa, Tatsuhiko Miyajima, Masakazu Arai, Hajime Kuno, Atsushi Narimatsu, Hisashi Hashimoto, Yasuhiro Int J Alzheimers Dis Research Article We have established high-throughput lectin-antibody ELISAs to measure different glycans on transferrin (Tf) in cerebrospinal fluid (CSF) using lectins and an anti-transferrin antibody (TfAb). Lectin blot and precipitation analysis of CSF revealed that PVL (Psathyrella velutina lectin) bound an unique N-acetylglucosamine-terminated N-glycans on “CSF-type” Tf whereas SSA (Sambucus sieboldiana agglutinin) bound α2,6-N-acetylneuraminic acid-terminated N-glycans on “serum-type” Tf. PVL-TfAb ELISA of 0.5 μL CSF samples detected “CSF-type” Tf but not “serum-type” Tf whereas SSA-TfAb ELISA detected “serum-type” Tf but not “CSF-type” Tf, demonstrating the specificity of the lectin-TfAb ELISAs. In idiopathic normal pressure hydrocephalus (iNPH), a senile dementia associated with ventriculomegaly, amounts of the SSA-reactive Tf were significantly higher than in non-iNPH patients, indicating that Tf glycan analysis by the high-throughput lectin-TfAb ELISAs could become practical diagnostic tools for iNPH. The lectin-antibody ELISAs of CSF proteins might be useful for diagnosis of the other neurological diseases. SAGE-Hindawi Access to Research 2011 2011-08-17 /pmc/articles/PMC3160710/ /pubmed/21876827 http://dx.doi.org/10.4061/2011/352787 Text en Copyright © 2011 Keiro Shirotani et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Shirotani, Keiro
Futakawa, Satoshi
Nara, Kiyomitsu
Hoshi, Kyoka
Saito, Toshie
Tohyama, Yuriko
Kitazume, Shinobu
Yuasa, Tatsuhiko
Miyajima, Masakazu
Arai, Hajime
Kuno, Atsushi
Narimatsu, Hisashi
Hashimoto, Yasuhiro
High Throughput ELISAs to Measure a Unique Glycan on Transferrin in Cerebrospinal Fluid: A Possible Extension toward Alzheimer's Disease Biomarker Development
title High Throughput ELISAs to Measure a Unique Glycan on Transferrin in Cerebrospinal Fluid: A Possible Extension toward Alzheimer's Disease Biomarker Development
title_full High Throughput ELISAs to Measure a Unique Glycan on Transferrin in Cerebrospinal Fluid: A Possible Extension toward Alzheimer's Disease Biomarker Development
title_fullStr High Throughput ELISAs to Measure a Unique Glycan on Transferrin in Cerebrospinal Fluid: A Possible Extension toward Alzheimer's Disease Biomarker Development
title_full_unstemmed High Throughput ELISAs to Measure a Unique Glycan on Transferrin in Cerebrospinal Fluid: A Possible Extension toward Alzheimer's Disease Biomarker Development
title_short High Throughput ELISAs to Measure a Unique Glycan on Transferrin in Cerebrospinal Fluid: A Possible Extension toward Alzheimer's Disease Biomarker Development
title_sort high throughput elisas to measure a unique glycan on transferrin in cerebrospinal fluid: a possible extension toward alzheimer's disease biomarker development
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3160710/
https://www.ncbi.nlm.nih.gov/pubmed/21876827
http://dx.doi.org/10.4061/2011/352787
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