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作 者:李晖[1] 王全立[2] 孙红琰[1] 詹林盛[1] 周勇[1] 彭剑淳[1]
机构地区:[1]军事医学科学院野战输血研究所 [2]军事医学科学院附属医院输血科,北京100071
出 处:《军事医学科学院院刊》2007年第1期20-23,共4页Bulletin of the Academy of Military Medical Sciences
摘 要:目的:制备并纯化HLA-B*2705-β2微球蛋白(β2-microglobulin,β2m)-多肽复合物。方法:将pET21 a-HLA-B*2705和pET21 a-β2m质粒在宿主菌E.coliBL21(DE3)中诱导表达,高效表达的HLA-B*2705蛋白与β2m,在HLA-B*2705限制性抗原肽〔来源于人类免疫缺陷病毒(H IV)gp120蛋白的九肽NH2-GRAFVTIGK-COOH〕存在的情况下,通过稀释复性折叠成HLA-B*2705-β2m-多肽复合物单体,经Western印迹鉴定,分子筛纯化。结果:成功地制备出HLA-B*2705-β2m-多肽复合物。结论:HLA-B*2705-β2m-多肽复合物的成功制备及纯化,为进一步研究HLA-B*2705与NK细胞Ig样受体(killer Ig-like receptor,KIR)之间的相互作用奠定了基础。Objective: To prepare and purify HLA-B * 2705-β2m-peptide complex. Methods: pET21a-HLA-B * 2705 And pET21a-β2m were transformed into E. eoli BL21, respectively, and their expression was induced by IPTG. The protein expressed was purified and refolded in vitro by limiting dilution with HLA-B * 2705, β2m and HLA-2705 binding peptide (NH2-GRAFVTIGK-COOH from the gp120 protein of HIV) to produce the HLA-B * 2705-β2m-peptide monomer. The product was detected by Western blot. Results: The experimental results showed that the protein of HLA-B * 2705-β2m- peptide complex was successfully constructed and refolded. Conclusion:The highly efficient expression of this protein lays the foundation for the further studies on exploration of the mechanism of immunization recognition between HLA-B * 2705 and killer Ig-like receptor of natural killer cell.
关 键 词:HLA-B*2705-β2m-多肽复合物 原核表达 纯化
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