journal article·2008-10-28Open access

Carbon Nanotubes Protect DNA Strands during Cellular Delivery

Yanrong Wu, Joseph A. Phillips, Haipeng Liu, Ronghua Yang, Weihong Tan

ACS Nano· Volume 2· Issue 10

Abstract

To protect against nuclease digestion, or single-strand binding protein interactions, oligonucleotides for targeted delivery into intracellular systems must be stable. To accomplish this, we have developed single-walled carbon nanotubes as a carrier for single-stranded DNA probe delivery. This has resulted in superior biostability for intracellular application and, hence, has achieved the desired protective attributes, which are particularly important when DNA probes are used for intracellular measurements. Specifically, when bound to single-walled carbon nanotubes, DNA probes are protected from enzymatic cleavage and interference from nucleic acid binding proteins. Moreover, and equally important, our study shows that a single-walled carbon nanotube-modified DNA probe, which targets a specific mRNA inside living cells, has increased self-delivery capability and intracellular biostability when compared to free DNA probes. Therefore, this new conjugate provides significant advantages for basic genomic studies in which DNA probes are used to monitor intracellular levels of molecules.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Advanced biosensing and bioanalysis techniques · RNA Interference and Gene Delivery · Nanopore and Nanochannel Transport Studies

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Center for Research at Bio/nano Interface, Department of Chemistry and Department of Physiology and Functional Genomics, Shands Cancer Center, UF Genetics Institute and McKnight Brain Institute, University of Florida, Gainesville, Florida 32611-7200,

Biomedical Engineering Center, State Key Lab of Chemo/Biosensing and Chemometrics, College of Chemistry and Chemical Engineering, Hunan University, Changsha 410082, China

References (22)

Show source-provided references
1. Sokolova V. · Angew. Chem., Int. Ed. · 2008 · 47 · 138210.1002/anie.200703039 ↗
2. He X. X. · J. Am. Chem. Soc. · 2003 · 125 · 716810.1021/ja034450d ↗
3. Martin C. R. · Nat. Rev. Drug Discovery · 2003 · 2 · 2910.1038/nrd988 ↗
4. Cui X. J. · Adv. Mater. · 2004 · 16 · 110910.1002/adma.200400081 ↗
5. Pantarotto D. · Chem. Commun. · 2004 · 1610.1039/b311254c ↗
6. Pantarotto D. · Angew. Chem., Int. Ed. · 2004 · 43 · 524210.1002/anie.200460437 ↗
7. Cai D. · Nat. Methods · 2005 · 2 · 44910.1038/nmeth761 ↗
8. Chen C. C. · Adv. Mater. · 2005 · 17 · 40410.1002/adma.200400966 ↗
9. Kwon N. H. · Nano Lett. · 2007 · 7 · 271810.1021/nl071179f ↗
10. Hampton T. · JAMA · 2007 · 298 · 505
11. Seferos D. S. · J. Am. Chem. Soc. · 2007 · 129 · 1547710.1021/ja0776529 ↗
12. Liu Z. · Angew. Chem., Int. Ed. · 2007 · 46 · 202310.1002/anie.200604295 ↗
13. Kam N. W. S. · Proc. Natl. Acad. Sci. U.S.A. · 2005 · 102 · 1160010.1073/pnas.0502680102 ↗
14. Heller D. A. · Science · 2006 · 311 · 50810.1126/science.1120792 ↗
15. Medley C. D. · Anal. Chem. · 2005 · 77 · 471310.1021/ac050881y ↗
16. Zheng M. · Nat. Mater. · 2003 · 2 · 33810.1038/nmat877 ↗
17. Yang R. · J. Am. Chem. Soc. · 2008 · 130 · 835110.1021/ja800604z ↗
18. Nakayama-Ratchford N. · J. Am. Chem. Soc. · 2007 · 129 · 244810.1021/ja068684j ↗
19. Li J. W. J. · Angew. Chem., Int. Ed. · 2000 · 39 · 104910.1002/(SICI)1521-3773(20000317)39:6<1049::AID-ANIE1049>3.0.CO;2-2 ↗
20. Wu Y. · Anal. Chem. · 2008 · 80 · 302510.1021/ac702637w ↗
21. Uchiyama H. · J. Biol. Chem. · 1996 · 271 · 38010.1074/jbc.271.1.380 ↗
22. Tyagi S. · Biophys. J. · 2004 · 87 · 415310.1529/biophysj.104.045153 ↗