<p>The specificity of anti-G-protein-coupled receptor (GPCR) antibodies has been tested in knockout animals; many of these antibodies are nonspecific (Pradidarcheep et al. 2009). Due to the lack of specific antibodies against the GPCR proteins, tissue distribution and subcellular localization of endogenous GPCR proteins in their native state are largely unknown. Anti-neuropeptide Y Y<sub>5</sub> receptor antibody, which did not react with Y<sub>5</sub> knockout brain tissue, revealed Y<sub>5</sub>-immunoreactivities as dot-like structures adjacent to the plasma membrane in the wild-type brain tissues (Murase et al. 2017). Here, we examined the expression pattern of endogenous neuropeptide Y Y<sub>1</sub> receptor using an anti-Y<sub>1</sub> antibody, the specificity of which was validated by a Y<sub>1</sub> knockout mouse. The anti-Y<sub>1</sub> antibody reacted with the wild-type brain sections and detected Y<sub>1</sub>-immunoreactivities. Y<sub>1</sub>/Y<sub>5</sub> double-positive neurons were observed in most brain regions examined here. In these neurons, Y<sub>1</sub> immunoreactivities appeared as dot-like structures, as did Y<sub>5</sub>. The anti-Y<sub>1</sub> antibody recognized the intracellular part of endogenous Y<sub>1</sub> molecules rather than the cell membrane-bound form, indicating the difficulties and demand for establishing antibodies against the physiologically active form of Y<sub>1</sub> molecules in vivo.</p>

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Neuropeptide Y Y1 receptor localization in mouse brain tissue revealed by an antibody with “hard specificity criterion”

  • Shin-ichi Murase

摘要

The specificity of anti-G-protein-coupled receptor (GPCR) antibodies has been tested in knockout animals; many of these antibodies are nonspecific (Pradidarcheep et al. 2009). Due to the lack of specific antibodies against the GPCR proteins, tissue distribution and subcellular localization of endogenous GPCR proteins in their native state are largely unknown. Anti-neuropeptide Y Y5 receptor antibody, which did not react with Y5 knockout brain tissue, revealed Y5-immunoreactivities as dot-like structures adjacent to the plasma membrane in the wild-type brain tissues (Murase et al. 2017). Here, we examined the expression pattern of endogenous neuropeptide Y Y1 receptor using an anti-Y1 antibody, the specificity of which was validated by a Y1 knockout mouse. The anti-Y1 antibody reacted with the wild-type brain sections and detected Y1-immunoreactivities. Y1/Y5 double-positive neurons were observed in most brain regions examined here. In these neurons, Y1 immunoreactivities appeared as dot-like structures, as did Y5. The anti-Y1 antibody recognized the intracellular part of endogenous Y1 molecules rather than the cell membrane-bound form, indicating the difficulties and demand for establishing antibodies against the physiologically active form of Y1 molecules in vivo.