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Generation and characterization of new monoclonal antibodies targeting the PHF1 and AT8 epitopes on human tau
by
Golde, Todd E.
, Riffe, Cara
, Strang, Kevin H.
, Goodwin, Marshall S.
, Chakrabarty, Paramita
, Moore, Brenda D.
, Levites, Yona
, Giasson, Benoit I.
in
Alzheimer Disease - metabolism
/ Alzheimer Disease - pathology
/ Alzheimer's disease
/ Amino acids
/ Analysis
/ Animals
/ Antibodies
/ Antibodies, Monoclonal
/ Antigenic determinants
/ Biomedical and Life Sciences
/ Biomedicine
/ Brain
/ Brain - metabolism
/ Brain - pathology
/ Cell Line, Tumor
/ Cloning
/ Dementia
/ Disease Models, Animal
/ Epitopes
/ Female
/ Genetic engineering
/ Humans
/ Hybridomas - metabolism
/ Immunization
/ Immunoglobulins
/ Immunohistochemistry
/ Immunotherapy
/ Laboratories
/ Medical research
/ Medicine, Experimental
/ Mice, Inbred BALB C
/ Mice, Transgenic
/ Monoclonal antibodies
/ Mutation
/ Nervous system diseases
/ Neurology
/ Neurosciences
/ Pathology
/ Peptides
/ Phosphorylation
/ Proteins
/ Recombinant Proteins - metabolism
/ Rodents
/ Tau
/ tau Proteins - deficiency
/ tau Proteins - genetics
/ tau Proteins - immunology
/ Transgenic mice
2017
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Generation and characterization of new monoclonal antibodies targeting the PHF1 and AT8 epitopes on human tau
by
Golde, Todd E.
, Riffe, Cara
, Strang, Kevin H.
, Goodwin, Marshall S.
, Chakrabarty, Paramita
, Moore, Brenda D.
, Levites, Yona
, Giasson, Benoit I.
in
Alzheimer Disease - metabolism
/ Alzheimer Disease - pathology
/ Alzheimer's disease
/ Amino acids
/ Analysis
/ Animals
/ Antibodies
/ Antibodies, Monoclonal
/ Antigenic determinants
/ Biomedical and Life Sciences
/ Biomedicine
/ Brain
/ Brain - metabolism
/ Brain - pathology
/ Cell Line, Tumor
/ Cloning
/ Dementia
/ Disease Models, Animal
/ Epitopes
/ Female
/ Genetic engineering
/ Humans
/ Hybridomas - metabolism
/ Immunization
/ Immunoglobulins
/ Immunohistochemistry
/ Immunotherapy
/ Laboratories
/ Medical research
/ Medicine, Experimental
/ Mice, Inbred BALB C
/ Mice, Transgenic
/ Monoclonal antibodies
/ Mutation
/ Nervous system diseases
/ Neurology
/ Neurosciences
/ Pathology
/ Peptides
/ Phosphorylation
/ Proteins
/ Recombinant Proteins - metabolism
/ Rodents
/ Tau
/ tau Proteins - deficiency
/ tau Proteins - genetics
/ tau Proteins - immunology
/ Transgenic mice
2017
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Generation and characterization of new monoclonal antibodies targeting the PHF1 and AT8 epitopes on human tau
by
Golde, Todd E.
, Riffe, Cara
, Strang, Kevin H.
, Goodwin, Marshall S.
, Chakrabarty, Paramita
, Moore, Brenda D.
, Levites, Yona
, Giasson, Benoit I.
in
Alzheimer Disease - metabolism
/ Alzheimer Disease - pathology
/ Alzheimer's disease
/ Amino acids
/ Analysis
/ Animals
/ Antibodies
/ Antibodies, Monoclonal
/ Antigenic determinants
/ Biomedical and Life Sciences
/ Biomedicine
/ Brain
/ Brain - metabolism
/ Brain - pathology
/ Cell Line, Tumor
/ Cloning
/ Dementia
/ Disease Models, Animal
/ Epitopes
/ Female
/ Genetic engineering
/ Humans
/ Hybridomas - metabolism
/ Immunization
/ Immunoglobulins
/ Immunohistochemistry
/ Immunotherapy
/ Laboratories
/ Medical research
/ Medicine, Experimental
/ Mice, Inbred BALB C
/ Mice, Transgenic
/ Monoclonal antibodies
/ Mutation
/ Nervous system diseases
/ Neurology
/ Neurosciences
/ Pathology
/ Peptides
/ Phosphorylation
/ Proteins
/ Recombinant Proteins - metabolism
/ Rodents
/ Tau
/ tau Proteins - deficiency
/ tau Proteins - genetics
/ tau Proteins - immunology
/ Transgenic mice
2017
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Generation and characterization of new monoclonal antibodies targeting the PHF1 and AT8 epitopes on human tau
Journal Article
Generation and characterization of new monoclonal antibodies targeting the PHF1 and AT8 epitopes on human tau
2017
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Overview
Tauopathies are a group of neurodegenerative disorders, including Alzheimer’s disease, defined by the presence of brain pathological inclusions comprised of abnormally aggregated and highly phosphorylated tau protein. The abundance of brain tau aggregates correlates with disease severity and select phospho-tau epitopes increase at early stages of disease. We generated and characterized a series of novel monoclonal antibodies directed to tau phosphorylated at several of these phospho-epitopes, including Ser396/Ser404, Ser404 and Thr205. We also generated phosphorylation independent antibodies against amino acid residues 193–211. We show that most of these antibodies are highly specific for tau and strongly recognize pathological inclusions in human brains and in a transgenic mouse model of tauopathy. They also reveal epitope-specific differences in the biochemical properties of Alzheimer’s disease sarkosyl-insoluble tau. These new reagents will be useful for investigating the progression of tau pathology and further as tools to target the cellular transmission of tau pathology.
Publisher
BioMed Central,BioMed Central Ltd,Nature Publishing Group,BMC
Subject
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