Lapa Sergey A, Chudinov Alexander V, Timofeev Edward N
Engelhardt Institute of Molecular Biology, Russian Academy of Sciences, Moscow, Russia.
Mol Biotechnol. 2016 Feb;58(2):79-92. doi: 10.1007/s12033-015-9907-9.
Aptamers are nucleic acid-based scaffolds that can bind with high affinity to a variety of biological targets. Aptamers are identified from large DNA or RNA libraries through a process of directed molecular evolution (SELEX). Chemical modification of nucleic acids considerably increases the functional and structural diversity of aptamer libraries and substantially increases the affinity of the aptamers. Additionally, modified aptamers exhibit much greater resistance to biodegradation. The evolutionary selection of modified aptamers is conditioned by the possibility of the enzymatic synthesis and replication of non-natural nucleic acids. Wild-type or mutant polymerases and their non-natural nucleotide substrates that can support SELEX are highlighted in the present review. A focus is made on the efforts to find the most suitable type of nucleotide modifications and the engineering of new polymerases. Post-SELEX modification as a complementary method will be briefly considered as well.
适体是基于核酸的支架,能够与多种生物靶点高亲和力结合。适体是通过定向分子进化过程(SELEX)从大型DNA或RNA文库中筛选出来的。核酸的化学修饰显著增加了适体文库的功能和结构多样性,并大幅提高了适体的亲和力。此外,修饰后的适体对生物降解表现出更强的抗性。修饰适体的进化选择取决于非天然核酸的酶促合成和复制的可能性。本综述重点介绍了能够支持SELEX的野生型或突变型聚合酶及其非天然核苷酸底物。重点在于寻找最合适的核苷酸修饰类型和新型聚合酶的工程改造。后SELEX修饰作为一种补充方法也将简要讨论。