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High-throughput site-directed mutagenesis using oligonucleotides synthesized on DNA chips

机译:使用在DNA芯片上合成的寡核苷酸进行高通量定点诱变

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摘要

Site-directed mutagenesis has greatly helped researchers both to understand the precise role of specific residues in coding sequences and to generate variants of proteins that have acquired new characteristics. Today's demands for more complete functional cartographies of proteins and advances in selection and screening technologies require that site-directed mutagenesis be adapted for high-throughput applications. We describe here the first generation of a library of single and multiple site-directed mutants using a mixture of oligonucleotides synthesized on DNA chips. We have used the human interleukin 15 (IL15) gene as a model, of which 37 codons were simultaneously targeted for substitution by any of eight possible codons. Ninety-six clones were sequenced, exhibiting a broad spectrum of targeted substitutions over the whole gene length with no unwanted mutations. Libraries produced using such pools of oligonucleotides open new perspectives to direct the evolution of proteins in vitro, by enabling the simple, rapid, and cost-effective generation of large tailor-made genetic diversities from any gene.
机译:定点诱变极大地帮助研究人员了解了特定残基在编码序列中的精确作用,并产生了具有新特性的蛋白质变体。如今,对更完整的蛋白质功能图谱的需求以及选择和筛选技术的进步要求对定点诱变进行调整,使其适合高通量应用。我们在这里描述了第一代使用DNA芯片上合成的寡核苷酸混合物的单一和多个定点突变体的库。我们已使用人类白介素15(IL15)基因作为模型,其中37个密码子同时被8个可能的密码子中的任何一个靶向。对九十六个克隆进行了测序,显示出在整个基因长度上无目标突变的广谱靶向取代。使用这种寡核苷酸库生产的文库,可以通过任何基因简单,快速且经济高效地生成大量量身定制的遗传多样性,从而为指导体外蛋白质的进化开辟了新的前景。

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