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Expression purification and bioactivity of GST-fused v-Src from a bacterial expression system

机译:来自细菌表达系统的GST融合v-Src的表达纯化和生物活性

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摘要

v-Src is a non-receptor protein tyrosine kinase involved in many signal transduction pathways and closely related to the activation and development of cancers. We present here the expression, purification, and bioactivity of a GST (glutathione S-transferase)-fused v-Src from a bacterial expression system. Different culture conditions were examined in an isopropyl β-D-thiogalactopyranoside (IPTG)-regulated expression, and the fused protein was purified using GSH (glutathione) affinity chromatography. ELISA (enzyme-linked immunosorbent assay) was employed to determine the phosphorylation kinase activity of the GST-fused v-Src. This strategy seems to be more promising than the insect cell system or other eukaryotic systems employed in earlier Src expression.
机译:v-Src是一种非受体蛋白酪氨酸激酶,参与许多信号转导途径,与癌症的激活和发展密切相关。我们在这里介绍从细菌表达系统的GST(谷胱甘肽S-转移酶)融合的v-Src的表达,纯化和生物活性。在异丙基β-D-硫代半乳糖吡喃糖苷(IPTG)调节的表达中检查了不同的培养条件,并使用GSH(谷胱甘肽)亲和色谱法纯化了融合蛋白。 ELISA(酶联免疫吸附测定)用于确定融合了GST的v-Src的磷酸化激酶活性。这种策略似乎比早期Src表达中使用的昆虫细胞系统或其他真核系统更有希望。

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