Vlasova I E, Vlasov V V
Mol Biol (Mosk). 1993 Jan-Feb;27(1):5-13.
Method of designing nucleic acids capable of specific complex formation with arbitrary ligands (aptamers) and catalytically competent nucleic acids are described. The methods rely on generation of libraries of random nucleotide sequences, selection of molecules possessing the desired property from these libraries, and amplification of the selected molecules. Repeating of the selection and amplification procedures results in evolutional improvement of the molecule ability to accomplish the function under consideration. This molecular evolution approach opens up broad possibilities for investigation of mechanisms of molecular recognition of small ligands and biopolymers by nucleic acids and mechanisms of reactions catalyzed by ribozymes. Design of novel ribozymes and nucleic acids capable of specific binding to certain biopolymers may become an efficient approach for development of practically important compounds, biologically active compounds and affinity sorbents.
描述了能够与任意配体特异性形成复合物的核酸(适配体)和具有催化活性的核酸的设计方法。这些方法依赖于随机核苷酸序列文库的生成、从这些文库中选择具有所需特性的分子以及所选分子的扩增。重复选择和扩增程序会导致分子完成所考虑功能的能力得到进化改进。这种分子进化方法为研究核酸对小配体和生物聚合物的分子识别机制以及核酶催化的反应机制开辟了广阔的可能性。设计能够与某些生物聚合物特异性结合的新型核酶和核酸可能成为开发实际重要化合物、生物活性化合物和亲和吸附剂的有效方法。