杆状病毒感染昆虫细胞培养中重组成纤维细胞生长因子受体的定量测定。

Receptor Pub Date : 1994-01-01
J L Duke, S P Sheth, A T Nahapetian
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引用次数: 0

摘要

成纤维细胞生长因子蛋白家族的成员参与了几个重要的生物学过程,包括血管生成、伤口愈合、肿瘤生长和转移。碱性成纤维细胞生长因子(bFGF)及其受体的相互作用具有重要的药理意义。为了研究其与碱性成纤维细胞生长因子受体1型(bFGFR1)相互作用的能量学,我们尝试生产克量的可溶性细胞外形式。本研究的目的是建立一种监测大规模杆状病毒感染昆虫细胞培养过程中bFGFR1浓度变化的方法。建立了一种简单的反相高效液相色谱法,用于直接测定昆虫细胞培养基中分泌的可溶性受体。该方法允许含有不同量的胎牛血清和bFGFR1 (10-30 mg/L)的细胞培养样品进行分析,而无需事先纯化。添加受体在1 ~ 7微克范围内呈线性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Quantitative determination of recombinant fibroblast growth factor receptor in baculovirus-infected insect cell cultures.

Members of the fibroblast growth factor protein family are involved in several biologically important processes, including angiogenesis, wound healing, and tumor growth and metastasis. Interactions of basic fibroblast growth factor (bFGF) and its receptors are of considerable pharmacological importance. Attempts were made to produce gram quantities of a soluble extracellular form of basic fibroblast growth factor receptor type 1 (bFGFR1) in order to study the energetics of its interaction with bFGF. The aim of the present study was to develop a method for monitoring changes in concentration of bFGFR1 during its production by large-scale baculovirus-infected insect cell culture. A simple reverse-phase high-performance liquid chromatographic assay was developed for direct determination of the soluble receptor secreted into insect cell-culture media. The method permitted cell-culture samples containing varying amounts of fetal calf serum and bFGFR1 (10-30 mg/L) to be analyzed without prior purification. The assay was linear for added receptor in the range of 1-7 micrograms.

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