摘要
拟南芥VSP1蛋白是一种具有酸性磷酸酶活性的植物防御蛋白。为利用硒原子的反常散射获取VSP1蛋白晶体X射线衍射的相位信息,以质粒pET-22b为表达载体,大肠杆菌B834(DE3)为宿主菌,在含有硒代甲硫氨酸的M9培养基中诱导表达VSP1硒代蛋白衍生物。通过Ni-NTA亲和层析纯化的目的蛋白经SDS-PAGE检验,纯度在95%以上。通过优化VSP1母体蛋白晶体的生长条件,获得了可衍射的硒代蛋白晶体。
Arabidopsis thaliana VSP1 is a defense protein with acid phosphatase activity. For the use of anomalous X-ray scattering of selenium to provide phase information, VSP1 selenium protein derivatives was expressed using pET-22b in E. coli B834 in M9 medium containing Se-Met. The target protein was purified using Ni-NTA resin and analyzed by SDS-PAGE. The purity was over 95%. The Se-Met-labeled VSP1 crystals were obtained by optimizing the condition of the native crystals.
出处
《生物学杂志》
CAS
CSCD
2011年第6期23-25,共3页
Journal of Biology
基金
国家自然科学基金(30970565)
安徽高校省级自然科学研究项目(KJ2009A177)
关键词
VSP1硒代蛋白衍生物
表达
纯化
晶体生长
VSP1 selenium protein derivatives
expression
purification
crystal growth