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Structure-guided development of Pb(2+)-binding DNA aptamers

Owing to its great threat to human health and environment, Pb(2+) pollution has been recognized as a major public problem by the World Health Organization (WHO). Many DNA aptamers have been utilized in the development of Pb(2+)-detection sensors, but the underlying mechanisms remain elusive. Here, w...

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Detalles Bibliográficos
Autores principales: Liu, Hehua, Gao, Yanqing, Mathivanan, Johnsi, Shen, Fusheng, Chen, Xi, Li, Yangyang, Shao, Zhiwei, Zhang, Yixi, Shao, Qiyuan, Sheng, Jia, Gan, Jianhua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8748701/
https://www.ncbi.nlm.nih.gov/pubmed/35013452
http://dx.doi.org/10.1038/s41598-021-04243-2
Descripción
Sumario:Owing to its great threat to human health and environment, Pb(2+) pollution has been recognized as a major public problem by the World Health Organization (WHO). Many DNA aptamers have been utilized in the development of Pb(2+)-detection sensors, but the underlying mechanisms remain elusive. Here, we report three Pb(2+)-complexed structures of the thrombin binding aptamer (TBA). These high-resolution crystal structures showed that TBA forms intramolecular G-quadruplex and Pb(2+) is bound by the two G-tetrads in the center. Compared to K(+)-stabilized G-quadruplexes, the coordinating distance between Pb(2+) and the G-tetrads are much shorter. The T3T4 and T12T13 linkers play important roles in dimerization and crystallization of TBA, but they are changeable for Pb(2+)-binding. In combination with mutagenesis and CD spectra, the G8C mutant structure unraveled that the T7G8T9 linker of TBA is also variable. In addition to expansion of the Pb(2+)-binding aptamer sequences, our study also set up one great example for quick and rational development of other aptamers with similar or optimized binding activity.