用重组融合蛋白分析trk NGF受体酪氨酸激酶。

C M Horvath, A Wolven, D Machadeo, J Huber, L Boter, M Benedetti, B Hempstead, M V Chao
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引用次数: 5

摘要

神经生长因子(NGF)是一类结构相关的营养因子,包括脑源性神经营养因子(BDNF)、神经营养因子-3 (NT-3)、NT-4和NT-5。这些神经营养因子与两类受体相互作用,trk受体酪氨酸激酶家族和低亲和力p75神经营养因子受体。为了研究潜在的配体-受体相互作用,构建了重组trk融合蛋白,并生成了针对细胞质酪氨酸激酶结构域的泛trk多克隆抗血清。评估重组蛋白的体外激酶活性和K-252a抑制磷酸化的能力。针对融合蛋白制备的抗体可以识别所有trk家族成员,并且在亲和交联受体的免疫沉淀中有效。比较交联表明NGF可以识别所有trk受体成员,说明神经营养因子与其受体之间存在大量潜在的配体-受体相互作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Analysis of the trk NGF receptor tyrosine kinase using recombinant fusion proteins.

Nerve growth factor (NGF) represents a family of structurally related trophic factors, including brain-derived neurotrophin factor (BDNF), neurotrophin-3 (NT-3), NT-4, and NT-5. These neurotrophin factors interact with two classes of receptors, the trk receptor tyrosine kinase family, and the low affinity p75 neurotrophin receptor. To study potential ligand-receptor interactions, recombinant trk fusion proteins have been constructed, and pan-trk polyclonal antisera directed against the cytoplasmic tyrosine kinase domain have been generated. The recombinant proteins were assessed for in vitro kinase activity and for the ability of K-252a to inhibit phosphorylation. Antibodies made against the fusion protein recognize all trk family members, and are effective in immunoprecipitation of affinity-crosslinked receptors. Comparative crosslinking indicates that NGF can recognize all trk receptor members, illustrating the large number of potential ligand-receptor interactions between neurotrophins and their receptors.

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