Inhibition of human APE1 and MTH1 DNA repair proteins by dextran-coated γ-Fe2O3 ultrasmall superparamagnetic iron oxide nanoparticles

Author:

Coskun Erdem1ORCID,Singh Neenu2ORCID,Scanlan Leona D3ORCID,Jaruga Pawel4ORCID,Doak Shareen H5ORCID,Dizdaroglu Miral4ORCID,Nelson Bryant C6ORCID

Affiliation:

1. Institute for Bioscience & Biotechnology Research, University of Maryland, Rockville, MD 20850, USA

2. Leicester School of Allied Health Sciences, Faculty of Health & Life Sciences, De Montfort University, The Gateway, Leicester, LE1 9BH, UK

3. California Environmental Protection Agency, Office of Environmental Health Hazard Assessment, 1001 I Street, Sacramento, CA 95814, USA

4. Biomolecular Measurement Division, National Institute of Standards & Technology, Gaithersburg, MD 20899, USA

5. Institute of Life Science, Center for NanoHealth, Swansea University Medical School, Wales, SA2 8PP, UK

6. Biosystems & Biomaterials Division, National Institute of Standards & Technology, Gaithersburg, MD 20899, USA

Abstract

Aim: To quantitatively evaluate the inhibition of human DNA repair proteins APE1 and MTH1 by dextran-coated γ-Fe2O3 ultrasmall superparamagnetic iron oxide nanoparticles (dUSPIONs). Materials & methods: Liquid chromatography–tandem mass spectrometry with isotope-dilution was used to measure the expression levels of APE1 and MTH1 in MCL-5 cells exposed to increasing doses of dUSPIONs. The expression levels of APE1 and MTH1 were measured in cytoplasmic and nuclear fractions of cell extracts. Results: APE1 and MTH1 expression was significantly inhibited in both cell fractions at the highest dUSPION dose. The expression of MTH1 was linearly inhibited across the full dUSPION dose range in both fractions. Conclusion: These findings warrant further studies to characterize the capacity of dUSPIONs to inhibit other DNA repair proteins in vitro and in vivo.

Publisher

Future Medicine Ltd

Subject

Development,General Materials Science,Biomedical Engineering,Medicine (miscellaneous),Bioengineering

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