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出 处:《第三军医大学学报》1999年第4期256-258,共3页Journal of Third Military Medical University
摘 要:目的:拟将噬菌粒pCOMB3改建为更为稳定、高拷贝且易于操作的噬菌体随机肽库载体。方法:对常用噬菌体抗体库呈现载体pCOMB3序列进行点矩阵作图分析(Dot-Plot分析),切除其中重复区,纠正其多代培养后自删除特性。原克隆位点63bp的填充序列增加到1435bp以便于酶切鉴定和电泳回收。结果:构建了命名为pTMB2的噬菌粒载体。结论:pTMB2的噬菌粒载体更为稳定且易于操作。Objective: To modify a combinational library display vector, pCOMB3 and to provide a stable, easily manipulated and highly copied vector for the display of a random peptide library. Methods: According to Dot Plot analysis of pCOMB3 nucleic acid sequences, the phagmid pCOMB3 was modified to eliminate the propensity of accumulated deletions in the region of cloning site. Furthermore, a 1375 bp DNA fragment from phage was cloned in the small 63 bp stuffer at the cloning site. Results: A 5129 vector named pTMB2 was produced. Conclusion: pTMB2 holds the appropriate characteristics for random peptide phage display with improved stability and ease of manipulation.
关 键 词:噬菌体随机肽库 pCOMB3 Dot-Plot分析 载体
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