Enhancement of In Vitro Translation by Gold Nanoparticle−DNA Conjugates
Source abstract
Abstract
Gold nanoparticle (AuNP)-DNA conjugates can enhance in vitro translation of a protein. Enhancement occurs via a combination of nonspecific adsorption of translation-related molecules and the ribosome to the AuNP-DNA and specific binding to the mRNA of interest. AuNP-DNA conjugates enhanced protein production of fluorescent proteins (mCherry, eGFP) in retic lysate mixes by 65-100%. Gel electrophoresis was used to probe nonspecific adsorption of the AuNP-DNA conjugates to the translation machinery. It was determined that nonspecific adsorption is critical for enhancement, and if it was eliminated, expression enhancement did not occur. The interaction of the mRNA with the DNA on the AuNP surface influenced the amount of enhancement and was probed by expression in the presence of RNase H. These results suggest that higher translation enhancement occurs when the DNA on the AuNP forms an incomplete duplex with the mRNA. Tuning the balance between nonspecific adsorption and specific binding of the AuNP-DNA conjugates could result in the translation enhancement of a specific gene in a mixture.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advanced biosensing and bioanalysis techniques · RNA Interference and Gene Delivery · DNA and Nucleic Acid Chemistry
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Mechanical Engineering
Department of Biological Engineering, Massachusetts Institute of Technology, 77 Massachusetts Avenue, Cambridge, Massachusetts 02139
References (37)
Show source-provided references
1. De M. · Adv. Mater. · 2008 · 20 · 422510.1002/adma.200703183 ↗
2. Alivisatos P. · Nat. Biotechnol. · 2004 · 22 · 4710.1038/nbt927 ↗
3. Medintz I. L. · Nat. Mater. · 2005 · 4 · 43510.1038/nmat1390 ↗
4. Thomas M. · Proc. Natl. Acad. Sci. U.S.A. · 2003 · 100 · 913810.1073/pnas.1233634100 ↗
5. Chen C.-C. · J. Am. Chem. Soc. · 2006 · 128 · 370910.1021/ja0570180 ↗
6. Loo C. · Nano Lett. · 2005 · 5 · 70910.1021/nl050127s ↗
7. Michalet X. · Science · 2005 · 307 · 53810.1126/science.1104274 ↗
8. Barhoumi A. · Chem. Phys. Lett. · 2009 · 482 · 17110.1016/j.cplett.2009.09.076 ↗
9. Braun G. B. · ACS Nano · 2009 · 3 · 200710.1021/nn900469q ↗
10. Lee S. E. · Nano Lett. · 2009 · 9 · 56210.1021/nl802689k ↗
11. Parak W. J. · Nano Lett. · 2003 · 3 · 3310.1021/nl025888z ↗
12. Aubin-Tam M.-E. · Proc. Natl. Acad. Sci. U.S.A. · 2009 · 106 · 409510.1073/pnas.0807299106 ↗
13. Nel A. E. · Nat. Mater. · 2009 · 8 · 54310.1038/nmat2442 ↗
14. Kimura-Suda H. · J. Am. Chem. Soc. · 2003 · 125 · 901410.1021/ja035756n ↗
15. Park S. · J. Phys. Chem. C · 2008 · 112 · 761110.1021/jp8004426 ↗
16. Brown K. A. · J. Phys. Chem. C · 2008 · 112 · 751710.1021/jp711869p ↗
17. Lee S. E. · J. Am. Chem. Soc. · 2009 · 131 · 1406610.1021/ja904326j ↗
18. Liu W. · J. Am. Chem. Soc. · 2008 · 130 · 127410.1021/ja076069p ↗
19. Zheng M. · Langmuir · 2004 · 20 · 422610.1021/la035981i ↗
20. Park S. · Nano Lett. · 2004 · 4 · 192510.1021/nl048920t ↗
21. Aubin-Tam M.-E. · Langmuir · 2005 · 21 · 1208010.1021/la052102e ↗
22. Otsuka H. · Adv. Drug Delivery Rev. · 2003 · 55 · 40310.1016/S0169-409X(02)00226-0 ↗
23. Choi H. S. · Nat. Nanotechnol. · 2010 · 5 · 4210.1038/nnano.2009.314 ↗
24. Fraser C. S. · Nat. Rev. Microbiol. · 2007 · 5 · 2910.1038/nrmicro1558 ↗
25. Fraser C. S. · Nat. Struct. Mol. Biol. · 2009 · 16 · 39710.1038/nsmb.1572 ↗
26. Gingras A.-C. · Annu. Rev. Biochem. · 1999 · 68 · 91310.1146/annurev.biochem.68.1.913 ↗
27. Ghosh P. S. · ACS Nano · 2008 · 2 · 221310.1021/nn800507t ↗
28. Dubertret B. · Nat. Biotechnol. · 2001 · 19 · 36510.1038/86762 ↗
29. Jason T. L. H. · Toxicol. Appl. Pharmacol. · 2004 · 201 · 6610.1016/j.taap.2004.04.017 ↗
30. Patil S. D. · AAPS J. · 2005 · 710.1208/aapsj070109 ↗
31. Rosi N. L. · Science · 2006 · 312 · 102710.1126/science.1125559 ↗
32. Walton S. P. · Biophys. J. · 2002 · 82 · 36610.1016/S0006-3495(02)75401-5 ↗
33. Nelson, D. L.; Cox, M. M.Lehninger Principles of Biochemistry,4th ed.;W. H. Freeman and Company:New York, 2005; pp288−289.
34. Beesley J. E. · 1989
35. Demers L. M. · Anal. Chem. · 2000 · 72 · 553510.1021/ac0006627 ↗
36. Shaner N. C. · Nat. Methods · 2005 · 2 · 90510.1038/nmeth819 ↗
37. Chalfie M. · Proc. Natl. Acad. Sci. U.S.A. · 2009 · 106