Klussmann S, Nolte A, Bald R, Erdmann V A, Fürste J P
Institut für Biochemie, Freie Universität Berlin, Germany.
Nat Biotechnol. 1996 Sep;14(9):1112-5. doi: 10.1038/nbt0996-1112.
A 58-mer L-RNA ligand that binds to naturally occurring D-adenosine with a dissociation constant of 1.7 microM in solution was identified from a combinatorial library employing mirror-design. The corresponding D-RNA ligand shows identical binding affinity to L-adenosine. Reciprocal chiral specificity was also evident from ligand discrimination; the binding affinity of the L-RNA ligand for D-adenosine was 9000-fold greater than its affinity for L-adenosine and vice versa. While the D-RNA ligand was rapidly degraded in human serum, the L-RNA ligand displayed an extraordinary stability. This indicates the potential application of specifically designed L-RNA ligands as stable monoclonal antibody analogues and the development of highly stable L-ribozymes.
通过镜像设计的组合文库,鉴定出一种58聚体的L-RNA配体,其在溶液中与天然存在的D-腺苷结合,解离常数为1.7微摩尔。相应的D-RNA配体对L-腺苷显示出相同的结合亲和力。配体识别也体现出相互的手性特异性;L-RNA配体对D-腺苷的结合亲和力比对L-腺苷的亲和力高9000倍,反之亦然。虽然D-RNA配体在人血清中迅速降解,但L-RNA配体表现出非凡的稳定性。这表明了经过特殊设计的L-RNA配体作为稳定的单克隆抗体类似物的潜在应用,以及高度稳定的L-核酶的开发。