Generation and Characterization of Specific Monoclonal Antibodies and Nanobodies Directed Against the ATP-Gated Channel P2X4

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Generation and Characterization of Specific Monoclonal Antibodies and Nanobodies Directed Against the ATP-Gated Channel P2X4. / Bergmann, Philine; Garcia de Paco, Elvira; Rissiek, Björn; Menzel, Stephan; Dubberke, Gudrun; Hua, Jennifer; Rassendren, François; Ulmann, Lauriane; Koch-Nolte, Friedrich.

In: FRONT CELL NEUROSCI, Vol. 13, 2019, p. 498.

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@article{59a13f73d3184eb5949ad70f5907b451,
title = "Generation and Characterization of Specific Monoclonal Antibodies and Nanobodies Directed Against the ATP-Gated Channel P2X4",
abstract = "The P2X4 channel is involved in different physiological and pathological conditions and functions in the nervous system. Despite the existence of several mouse models for which the expression of the gene was manipulated, there is still little information on the expression of the protein at the cellular level. In particular, supposedly specific available antibodies have often proved to recognize unrelated proteins in P2X4-deficient mice. Here, we used an in vivo DNA vaccine approach to generate a series of monoclonal antibodies and nanobodies specific for human, mouse, and rat P2X4 channels. We further characterized these antibodies and show that they solely recognize the native form of the proteins both in biochemical and cytometric applications. Some of these antibodies prove to specifically recognize P2X4 channels by immunostaining in brain or sensory ganglia slices, as well as at the cellular and subcellular levels. Due to their clonality, these different antibodies should represent versatile tools for further characterizing the cellular functions of P2X4 in the nervous system as well as at the periphery.",
author = "Philine Bergmann and {Garcia de Paco}, Elvira and Bj{\"o}rn Rissiek and Stephan Menzel and Gudrun Dubberke and Jennifer Hua and Fran{\c c}ois Rassendren and Lauriane Ulmann and Friedrich Koch-Nolte",
note = "Copyright {\textcopyright} 2019 Bergmann, Garcia de Paco, Rissiek, Menzel, Dubberke, Hua, Rassendren, Ulmann and Koch-Nolte.",
year = "2019",
doi = "10.3389/fncel.2019.00498",
language = "English",
volume = "13",
pages = "498",
journal = "FRONT CELL NEUROSCI",
issn = "1662-5102",
publisher = "Frontiers Media",

}

RIS

TY - JOUR

T1 - Generation and Characterization of Specific Monoclonal Antibodies and Nanobodies Directed Against the ATP-Gated Channel P2X4

AU - Bergmann, Philine

AU - Garcia de Paco, Elvira

AU - Rissiek, Björn

AU - Menzel, Stephan

AU - Dubberke, Gudrun

AU - Hua, Jennifer

AU - Rassendren, François

AU - Ulmann, Lauriane

AU - Koch-Nolte, Friedrich

N1 - Copyright © 2019 Bergmann, Garcia de Paco, Rissiek, Menzel, Dubberke, Hua, Rassendren, Ulmann and Koch-Nolte.

PY - 2019

Y1 - 2019

N2 - The P2X4 channel is involved in different physiological and pathological conditions and functions in the nervous system. Despite the existence of several mouse models for which the expression of the gene was manipulated, there is still little information on the expression of the protein at the cellular level. In particular, supposedly specific available antibodies have often proved to recognize unrelated proteins in P2X4-deficient mice. Here, we used an in vivo DNA vaccine approach to generate a series of monoclonal antibodies and nanobodies specific for human, mouse, and rat P2X4 channels. We further characterized these antibodies and show that they solely recognize the native form of the proteins both in biochemical and cytometric applications. Some of these antibodies prove to specifically recognize P2X4 channels by immunostaining in brain or sensory ganglia slices, as well as at the cellular and subcellular levels. Due to their clonality, these different antibodies should represent versatile tools for further characterizing the cellular functions of P2X4 in the nervous system as well as at the periphery.

AB - The P2X4 channel is involved in different physiological and pathological conditions and functions in the nervous system. Despite the existence of several mouse models for which the expression of the gene was manipulated, there is still little information on the expression of the protein at the cellular level. In particular, supposedly specific available antibodies have often proved to recognize unrelated proteins in P2X4-deficient mice. Here, we used an in vivo DNA vaccine approach to generate a series of monoclonal antibodies and nanobodies specific for human, mouse, and rat P2X4 channels. We further characterized these antibodies and show that they solely recognize the native form of the proteins both in biochemical and cytometric applications. Some of these antibodies prove to specifically recognize P2X4 channels by immunostaining in brain or sensory ganglia slices, as well as at the cellular and subcellular levels. Due to their clonality, these different antibodies should represent versatile tools for further characterizing the cellular functions of P2X4 in the nervous system as well as at the periphery.

U2 - 10.3389/fncel.2019.00498

DO - 10.3389/fncel.2019.00498

M3 - SCORING: Journal article

C2 - 31798414

VL - 13

SP - 498

JO - FRONT CELL NEUROSCI

JF - FRONT CELL NEUROSCI

SN - 1662-5102

ER -