Next Article in Journal
Magnetic Nanoparticle-Assisted Tunable Optical Patterns from Spherical Cholesteric Liquid Crystal Bragg Reflectors
Next Article in Special Issue
ZnO Nanowire Application in Chemoresistive Sensing: A Review
Previous Article in Journal
Rationally Controlled Synthesis of CdSexTe1−x Alloy Nanocrystals and Their Application in Efficient Graded Bandgap Solar Cells
Previous Article in Special Issue
ZnO Interactions with Biomatrices: Effect of Particle Size on ZnO-Protein Corona
Open AccessArticle

ZnO Nanoparticles Protect RNA from Degradation Better than DNA

1
Nanotechnology Innovation Center Kansas State (NICKS), Department of Anatomy and Physiology, College of Veterinary Medicine, Manhattan, KS 66506, USA
2
Department of Biomedical Sciences, College of Health and Human Services, Missouri State University, Springfield, MO 65897, USA
*
Author to whom correspondence should be addressed.
Nanomaterials 2017, 7(11), 378; https://doi.org/10.3390/nano7110378
Received: 22 September 2017 / Revised: 23 October 2017 / Accepted: 31 October 2017 / Published: 8 November 2017
(This article belongs to the Special Issue ZnO and TiO2 Based Nanostructures)
Gene therapy and RNA delivery require a nanoparticle (NP) to stabilize these nucleic acids when administered in vivo. The presence of degradative hydrolytic enzymes within these environments limits the nucleic acids’ pharmacologic activity. This study compared the effects of nanoscale ZnO and MgO in the protection afforded to DNA and RNA from degradation by DNase, serum or tumor homogenate. For double-stranded plasmid DNA degradation by DNase, our results suggest that the presence of MgO NP can protect DNA from DNase digestion at an elevated temperature (65 °C), a biochemical activity not present in ZnO NP-containing samples at any temperature. In this case, intact DNA was remarkably present for MgO NP after ethidium bromide staining and agarose gel electrophoresis where these same stained DNA bands were notably absent for ZnO NP. Anticancer RNA, polyinosinic-polycytidylic acid (poly I:C) is now considered an anti-metastatic RNA targeting agent and as such there is great interest in its delivery by NP. For it to function, the NP must protect it from degradation in serum and the tumor environment. Surprisingly, ZnO NP protected the RNA from degradation in either serum-containing media or melanoma tumor homogenate after gel electrophoretic analysis, whereas the band was much more diminished in the presence of MgO. For both MgO and ZnO NP, buffer-dependent rescue from degradation occurred. These data suggest a fundamental difference in the ability of MgO and ZnO NP to stabilize nucleic acids with implications for DNA and RNA delivery and therapy. View Full-Text
Keywords: DNase; RNase; DNase activity; RNase activity; metal oxide nanoparticle (MONP); gel electrophoresis; MgO; ZnO; DNA stability; RNA stability DNase; RNase; DNase activity; RNase activity; metal oxide nanoparticle (MONP); gel electrophoresis; MgO; ZnO; DNA stability; RNA stability
Show Figures

Graphical abstract

MDPI and ACS Style

McCall, J.; Smith, J.J.; Marquardt, K.N.; Knight, K.R.; Bane, H.; Barber, A.; DeLong, R.K. ZnO Nanoparticles Protect RNA from Degradation Better than DNA. Nanomaterials 2017, 7, 378.

Show more citation formats Show less citations formats
Note that from the first issue of 2016, MDPI journals use article numbers instead of page numbers. See further details here.

Article Access Map

1
Back to TopTop