Chem. J. Chinese Universities ›› 2018, Vol. 39 ›› Issue (11): 2445.doi: 10.7503/cjcu20180168

• Organic Chemistry • Previous Articles     Next Articles

Modification of Aptamer TBA with Extra Functional Groups and the Biological Activities

DU Shanshan1, LI Yang1, GUO Lei2, LI Pengyu1, CHAI Zhilong1, WANG Tao2, QUAN Dongqin2, HE Junlin2,*()   

  1. 1. School of Pharmaceutical Sciences, Guizhou University, Guizhou 550025, China
    2. Beijing Institute of Pharmacology and Toxicology, Beijing 100850, China
  • Received:2018-03-04 Online:2018-11-10 Published:2018-10-10
  • Contact: HE Junlin E-mail:hejunlin@bmi.ac.cn
  • Supported by:
    † Supported by the National Natural Science Foundation of China(No.21572268).

Abstract:

Thrombin binding aptamer(TBA) is a small aptamer for human α-thrombin. Detailed structural analysis has demonstrated that the two-layer G-quartet acts as the structural backbone and three loops have different contributions for the intramolecular stability and the interaction with thrombin. Here, the chemical modification with 5-[(2-aminoethyl)amino-2-oxoethyl]-2'-deoxythymidine(1) on the two loops of TBA(T3T12 and T4T13) were reported. The 5-substituent induced different effect for each residue in the loops. The intramolecular stacking of T4 and T13 were negatively affected for the thermal stability and the inhibitory activity. In the case of the loop T3 and T12 extruding outward, the extra functional groups of the compound 1 were helpful for the interaction with thrombin, the 5-positioned extra amino and amido groups were probably located at the right positions for the hydrogen bonding interaction with the residues from thrombin. These results further confirmed the loop residues for their folding positions, and their contributions could be enhanced by 5-substituted functional groups of 2'-deoxythymidine at specific positions.

Key words: Thrombin binding aptamer(TBA), Thermal stability, Circular dichroism, Clotting time

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