Cho J, Hamasaki K, Rando R R
Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, 250 Longwood Avenue, Boston, Massachusetts 02115, USA.
Biochemistry. 1998 Apr 7;37(14):4985-92. doi: 10.1021/bi972757h.
A small (40 nucleotides) stem-loop derivative (J6f1) of a specific aminoglycoside-binding RNA aptamer, containing a 3 nt and a 1 nt bulge, has previously been shown to stoichiometrically bind tobramycin with a dissociation constant of approximately 5 nM [Hamasaki, K., Killian, J., Cho, J. and Rando, R. R. (1997) Biochemistry 36, 1367-1371]. This construct can strongly discriminate among similar aminoglycosides with respect to binding. A combination of chemical interference studies, chemical modification studies, and mutational studies are performed to define the aminoglycoside binding site of J6f1. Recognition of the aminoglycoside by J6f1 involves contacts with nucleotide bases, rather than with the phosphate backbone. The binding site 1 comprised of part of the stem-loop region. The two bulges are also essential for high affinity and stoichiometric binding of tobramycin. These bulges are probably important for prying open the double helical region, thereby allowing the aminoglycoside access to the nucleotide bases.
一种特定的氨基糖苷结合RNA适配体的小(40个核苷酸)茎环衍生物(J6f1),含有一个3个核苷酸和一个1个核苷酸的凸起,先前已被证明以约5 nM的解离常数化学计量地结合妥布霉素[滨崎克、基利安J、赵J和兰多RR(1997年)《生物化学》36,1367 - 1371]。该构建体在结合方面能够强烈区分相似的氨基糖苷。进行了化学干扰研究、化学修饰研究和突变研究的组合,以确定J6f1的氨基糖苷结合位点。J6f1对氨基糖苷的识别涉及与核苷酸碱基的接触,而不是与磷酸骨架的接触。结合位点1由茎环区域的一部分组成。这两个凸起对于妥布霉素的高亲和力和化学计量结合也是必不可少的。这些凸起可能对于撬开双螺旋区域很重要,从而使氨基糖苷能够接触到核苷酸碱基。