溶性二元蛋白在体内结合PrP(Sc) 并对抗病
Philipp Meier1, Nicolas Genoud, Marco Prinz
1Institute of Neuropathology, Schmelzbergstrasse, University Hospital of Zürich, Zürich, Switzerland.
Cell
|April 8, 2003
概括
可溶性蛋白衍生物,如PrP-Fc2),可以阻止正常细胞蛋白 (PrP(C)) 转化为传染性PrP(Sc) 形式,从而抑制的复制和疾病.
科学领域:
- 神经科学是一个神经科学.
- 生物化学 生物化学
- 分子生物学分子生物学
背景情况:
- 细胞蛋白 (PrP(C)) 通过未知的机制转化为病理性PrP(Sc).
- 性疾病,如甲状腺炎,以PrP(Sc) 积累和神经退行为特征.
研究的目的:
- 研究可溶性蛋白衍生物在转化和疾病病原发生中的作用.
- 为了确定PrP-Fc(2) 是否可以在体内抑制子复制.
主要方法:
- 生成的转基因小鼠表达PrP(C) 与免疫球蛋白Fcgamma (PrP-Fc(2) 融合.
- 接种了感染性子的免疫小鼠,并监测了疾病的进展.
- 分析了PrP(Sc) 积累,代理物复制以及PrP-Fc(2) 在大脑中的定位和转化.
主要成果:
- 在野生型小鼠中,PrP-Fc(2) 表达延迟了PrP(Sc) 积累,病原体复制和疾病发病.
- PrP-Fc(2) 局部化在脂质上,与PrP(Sc) 相关,但抵抗转化.
- 缺乏内源 PrP ((C) 但表达 PrP-Fc ((2) 的小鼠耐受性较强,不会传播疾病.
结论:
- 通过抵抗转化,PrP-Fc(2) 干扰着子的传播和草病原发生.
- 可溶性蛋白衍生物显示出作为复制的新型抗体的潜力.
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