Protein Binding Effects of Dopamine Coated Titanium Dioxide Shell Nanoparticles

Author:

Lastra Ruben O.1ORCID,Paunesku Tatjana1ORCID,Gutama Barite1,Reyes Filiberto1,François Josie1,Martinez Shelby1,Xin Lun1ORCID,Brown Koshonna1ORCID,Zander Alia1ORCID,Raha Sumita1ORCID,Protic Miroslava1,Nanavati Dhaval2ORCID,Bi Yingtao3ORCID,Woloschak Gayle E4ORCID

Affiliation:

1. Department of Radiation Oncology, Northwestern University Feinberg School of Medicine

2. Proteomics Core, Northwestern University Chemistry of Life Processes Institute

3. Department of Biomedical Informatics, Northwestern University Feinberg School of Medicine

4. Northwestern University Feinberg School of Medicine

Abstract

Non-targeted nanoparticles are capable of entering cells, passing through different subcellular compartments and accumulating on their surface a protein corona that changes over time. In this study, we used metal oxide nanoparticles with iron-oxide core covered with titanium dioxide shell (Fe3O4@TiO2), with a single layer of covalently bound dopamine covering the nanoparticle surface. Mixing nanoparticles with cellular protein isolates showed that these nanoparticles can form complexes with numerous cellular proteins. The addition of non-toxic quantities of nano-particles to HeLa cell culture resulted in their non-specific uptake and accumulation of protein corona on nanoparticle surface. TfRC, Hsp90 and PARP were followed as representative protein components of nanoparticle corona; each protein bound to nanoparticles with different affinity. The presence of nanoparticles in cells also mildly modulated gene expression on the level of mRNA. In conclusion, cells exposed to non-targeted nanoparticles show subtle but numerous changes that are consistent from one experiment to another.

Funder

National Institutes of Health

Ames Research Center

National Foundation for Science and Technology Development

Publisher

Andover House Inc

Subject

General Medicine

Reference43 articles.

1. [1] E. J. Petersen et al., "Identification and Avoidance of Potential Artifacts and Misinterpre-tations in Nanomaterial Ecotoxicity Measurements," (in English), Environmental Science & Technology, Review vol. 48, no. 8, pp. 4226-4246, Apr 2014.

2. [2] M. P. Monopoli, C. Aberg, A. Salvati, and K. A. Dawson, "Biomolecular coronas pro-vide the biological identity of nanosized materials," Nat Nanotechnol, vol. 7, no. 12, pp. 779-86, Dec 2012.

3. [3] M. Lundqvist et al., "The evolution of the protein corona around nanoparticles: a test study," ACS Nano, vol. 5, no. 9, pp. 7503-9, Sep 27 2011.

4. [4] M. Karimi et al., "Smart micro/nanoparticles in stimulus-responsive drug/gene delivery systems," Chem Soc Rev, vol. 45, no. 5, pp. 1457-501, Mar 7 2016.

5. [5] V. Mirshafiee, M. Mahmoudi, K. Lou, J. Cheng, and M. L. Kraft, "Protein corona signif-icantly reduces active targeting yield," Chem Commun (Camb), vol. 49, no. 25, pp. 2557-9, Mar 28 2013.

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3