Crystal structures and identification of novel Cd2+-specific DNA aptamer

Author:

Liu Hehua1,Gao Yanqing1,Mathivanan Johnsi2,Armour-Garb Zev2,Shao Zhiwei1,Zhang Yixi1,Zhao Xin1,Shao Qiyuan1,Zhang Weizhen1,Yang Jie1,Cao Chulei1,Li Huili1,Sheng Jia2ORCID,Gan Jianhua1ORCID

Affiliation:

1. Shanghai Public Health Clinical Center, State Key Laboratory of Genetic Engineering, Collaborative Innovation Center of Genetics and Development, Department of Biochemistry and Biophysics, School of Life Sciences, Fudan University , Shanghai  200438, China

2. Department of Chemistry and The RNA Institute, University at Albany, State University of New York , Albany , NY  12222 , USA

Abstract

Abstract Cadmium (Cd) is one of the most toxic heavy metals. Exposure to Cd can impair the functions of the kidney, respiratory system, reproductive system and skeletal system. Cd2+-binding aptamers have been extensively utilized in the development of Cd2+-detecting devices; however, the underlying mechanisms remain elusive. This study reports four Cd2+-bound DNA aptamer structures, representing the only Cd2+-specific aptamer structures available to date. In all the structures, the Cd2+-binding loop (CBL-loop) adopts a compact, double-twisted conformation and the Cd2+ ion is mainly coordinated with the G9, C12 and G16 nucleotides. Moreover, T11 and A15 within the CBL-loop form one regular Watson–Crick pair and stabilize the conformation of G9. The conformation of G16 is stabilized by the G8–C18 pair of the stem. By folding and/or stabilizing the CBL-loop, the other four nucleotides of the CBL-loop also play important roles in Cd2+ binding. Similarly to the native sequence, crystal structures, circular dichroism spectrum and isothermal titration calorimetry analysis confirm that several variants of the aptamer can recognize Cd2+. This study not only reveals the underlying basis for the binding of Cd2+ ions with the aptamer, but also extends the sequence for the construction of novel metal–DNA complex.

Funder

National Natural Science Foundation of China

National Science Foundation

China Postdoctoral Science Foundation

Publisher

Oxford University Press (OUP)

Subject

Genetics

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