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首页> 外文期刊>Bulletin of the Korean Chemical Society >Aptamer-Based Precipitation as an Alternative to the Conventional Immunoprecipitation for Purification of Target Proteins
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Aptamer-Based Precipitation as an Alternative to the Conventional Immunoprecipitation for Purification of Target Proteins

机译:基于适体的沉淀法可替代常规免疫沉淀法纯化目标蛋白

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Aptamers are oligonucleotides or peptide molecules that are able to bind to their specific target molecules with high affinity via molecular recognition. In this study, we present development of aptamer-based precipitation assays (or simply aptamoprecipitation) for His-tagged proteins and thrombin to compare their purification efficiency with other conventional affinity precipitation methods. A crosslinking method was employed to immobilize thiol-functionalized aptamers onto the surface of polystyrene resins, enabling them to specifically bind to His-tag and to thrombin, respectively. The resulting aptamer-functionalized resins were successfully applied via a one-step experiment to purification of His-tagged proteins from complex E. coli and to thrombin extraction, exhibiting superior or at least comparable purification results to the conventional immobilized metal affinity precipitation or immunoprecipitation.
机译:适体是能够通过分子识别以高亲和力结合至其特定靶分子的寡核苷酸或肽分子。在这项研究中,我们介绍了针对His标记的蛋白和凝血酶的基于适体的沉淀分析(或简称为aptamoprecipitation)的开发,以将其纯化效率与其他常规亲和沉淀方法进行比较。采用交联方法将巯基官能化的适体固定在聚苯乙烯树脂的表面,使它们分别与His-tag和凝血酶特异性结合。通过一步实验成功地将所得的适体官能化树脂应用于从复杂大肠杆菌中纯化His-tagged蛋白和进行凝血酶提取,与常规固定化金属亲和沉淀或免疫沉淀法相比,具有更好的或至少可比的纯化结果。

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