Volume 76, Issue 1 pp. 85-92
research papers

Crystal engineering of an adenine–decavanadate molecular device towards label-free chemical sensing and biological screening

Sima Sedghiniya

Sima Sedghiniya

University of Tehran, School of Chemistry, College of Science, PO Box 14155-6455, Tehran, Iran

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Janet Soleimannejad

Corresponding Author

Janet Soleimannejad

University of Tehran, School of Chemistry, College of Science, PO Box 14155-6455, Tehran, Iran

Janet Soleimannejad, e-mail: [email protected]Search for more papers by this author
Zohreh Jahani

Zohreh Jahani

University of Tehran, Institute of Biochemistry and Biophysics, PO Box 14155-6455, Tehran, Iran

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Jamshid Davoodi

Jamshid Davoodi

University of Tehran, Institute of Biochemistry and Biophysics, PO Box 14155-6455, Tehran, Iran

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Jan Janczak

Jan Janczak

Polish Academy of Science, Institute of Low Temperature and Structure Research, PO Box 1410, Wroclaw, 50950 Poland

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First published: 06 February 2020

Abstract

Due to the inherent geometrical interdependencies of nucleic acid structures, the ability to engineer biosensors that rely on the specific interactions of these compounds is of considerable importance. Additionally, sensing or screening in a label-free fashion is a capability of these structures that can be readily achieved by exploiting the fluorescent component. In this work, the [AdH]6[V10O28].4(H2O) (1) supramolecular structure is introduced using adenine and decavanadate moieties that allow probing of selectivity to specific nucleic acid binding events by optical changes. The structure of (1) is an alternating organic–inorganic hybrid architecture of cationic adeninium (AdH+) ribbons and anionic decavanadate (DV)–water sheets. The luminescent screening and anticancer activity of compound (1) on the two human mammary carcinoma cell lines MDA-MB-231 and MCF7 were investigated using fluorescent microscopy and MTT assays, respectively. It was found that compound (1) is cell permeable with no toxicity below 12.5 µM concentration and moderate cytotoxicity at concentrations as high as 200 µM in human breast cancer cell lines, making it a useful tool to study the cell nucleus in real time.

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