Gong Xing-Guo, Ji Jing, Xie Jie, Zhou Yuan, Zhang Jun-Yan, Zhong Wen-Tao
Institute of Biomacromolecule and Enzyme Engineering, School of Life Sciences, Zhejiang University, Hangzhou 310027, China.
J Zhejiang Univ Sci B. 2006 Jan;7(1):13-9. doi: 10.1631/jzus.2006.B0013.
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 beta-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.
v-Src是一种非受体蛋白酪氨酸激酶,参与多种信号转导途径,与癌症的激活和发展密切相关。我们在此展示了从细菌表达系统中获得的谷胱甘肽S-转移酶(GST)融合v-Src的表达、纯化及生物活性。在异丙基β-D-硫代半乳糖苷(IPTG)调控的表达中检测了不同的培养条件,并使用谷胱甘肽(GSH)亲和层析法纯化融合蛋白。采用酶联免疫吸附测定(ELISA)来确定GST融合v-Src的磷酸化激酶活性。该策略似乎比早期Src表达中使用的昆虫细胞系统或其他真核系统更具前景。