Nanocrystals modified with peptide nucleic acids (PNAs) for selective self-assembly and DNA detection

Journal of the American Chemical Society

Volumn 125, Issue 41, 2003, Pages 12531-12540

  Chakrabarti, Raj ^a   Klibanov, Alexander M ^a  

^a MASSACHUSETTS INSTITUTE OF TECHNOLOGY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

HYBRIDIZATION;

BIOASSAY; BIOCHEMISTRY; COLORIMETRIC ANALYSIS; ELECTROSTATICS; NANOSTRUCTURED MATERIALS; PARTICLE SIZE ANALYSIS; SELF ASSEMBLY;

DNA;

GOLD; NANOPARTICLE; PEPTIDE NUCLEIC ACID;

ARTICLE; BASE MISPAIRING; COLORIMETRY; CRYSTAL STRUCTURE; DNA DETERMINATION; DNA HYBRIDIZATION; PROTEIN AGGREGATION; PROTEIN ASSEMBLY; PROTEIN MOTIF; PROTEIN PROTEIN INTERACTION; PROTEIN STABILITY; PROTEIN STRUCTURE; STRUCTURE ANALYSIS; SURFACE PROPERTY;

BASE PAIR MISMATCH; COLORIMETRY; DNA; GOLD; NANOTECHNOLOGY; NUCLEIC ACID HYBRIDIZATION; NYLONS; PARTICLE SIZE; PEPTIDE NUCLEIC ACIDS; SURFACE PROPERTIES;

EID: 0141988950     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja035399g     Document Type: Article

References (28)

1. Seeman, N. C. Nano Lett. 2001, 1, 22-25.
2. Mirkin, C. A.; Letsinger, R. L.; Mucic, R. C.; Storhoff, J. J. Nature 1996, 382, 607-609.
3. Mitchell, G. P.; Mirkin, C. A.; Letsinger, R. L. J. Am. Chem. Soc. 1999, 121, 8122-8123.
4. Well-ordered superlattices have been prepared by the evaporation of organic solvents from nanoparticles stabilized by nonpolar ligands, although this method is incapable of placing an arbitrary variety of distinct particles in predetermined locations. For a review, see Murray, C. B.; Kagan, C. R.; Bawendi, M. G. Annu. Rev. Mater. Sci. 2000, 30, 545-610.
5. Elghanian, R.; Storhoff, J. J.; Mucic, R. C.; Letsinger, R. L.; Mirkin, C. A. Science 1997, 277, 1078-1081.
6. Jin, R.; Wu, G.; Li, Z.; Mirkin, C. A.; Schatz, G. C. J. Am. Chem. Soc. 2003, 125, 1643-1654.
7. (a) Nielsen, P. E.; Egholm, M.; Buchardt, O. Bioconjugate Chem. 1994, 5, 3-7.
8. (b) Eriksson, M.; Nielsen, P. E. Q. Rev. Biophys. 1996, 29, 369-394.
9. (c) Uhlmann, E.; Peyman, A.; Breipohl, G.; Will, D. W. Angew. Chem., Int. Ed. 1998, 37, 2796-2823.
10. (d) Nielsen, P. E.; Egholm, M. Curr. Issues Mol. Biol. 1999, 1, 89-104.
11. Ganesh, K. N.; Nielsen, P. E. Curr. Org. Chem. 2000, 4, 941-943.
12. m > 30 °C.
13. Egholm, M.; Buchardt, O.; Nielsen, P. E.; Berg, R. H. J. Am. Chem. Soc. 1992, 114, 1895-1897.
14. a's can increase by up to 2 units.
15. Fritz, J.; Baller, M. K.; Lang, H. P.; Strunz, T.; Meyer, E.; Guntherodt, H.-J.; Delamarche, E.; Gerber, C.; Gimzewski, J. K. Langmuir 2000, 16, 9694-9696.
16. Loweth, C. J.; Caldwell, W. B.; Peng, X.; Alivisatos, A. P.; Schultz, P. G. Angew. Chem., Int. Ed. 1999, 38, 1808-1812.
17. Herne, T. M.; Tarlov, M. J. J. Am. Chem. Soc. 1997, 119, 8916-8920.
18. + resulted in essentially no attachment of DNA (data not shown). This method was therefore not applied to nanoparticles.
19. Bain, C. D.; Evall, J.; Whitesides, G. M. J. Am. Chem. Soc. 1989, 111, 7155-7164.
20. + for E, F, and DNA G).
21. Aoki, H.; Buhlmann, P.; Umezawa, Y. Electroanalysis 2000, 12, 1272-1276.
22. Demers, L. M.; Mirkin, C. A.; Mucic, R. C.; Reynolds, R. A.; Letsinger, R. L.; Elghanian, R.; Viswanadham, G. Anal. Chem. 2000, 72, 5535-5541.
23. Wang, J. Biosens. Bioelectron. 1998, 13, 757-762.
24. Mucic, R. C.; Storhoff, J. J.; Mirkin, C. A.; Letsinger, R. L. J. Am. Chem. Soc. 1998, 120, 12674-12675.
25. Wittung, P.; Nielsen, P. E.; Buchardt, O.; Egholm, M.; Norden, B. Nature 1994, 368, 561-563.
26. Seeman, N. C. Nature 2003, 421, 427-431.
27. Grabar, K. C.; Freeman, R. G.; Hommer, M. B.; Natan, M. J. Anal. Chem. 1995, 67, 735-743.
28. Practical Surface Analysis by Auger and X-ray Photoelectron Spectroscopy; Briggs, D., Seah, M. P., Eds. Wiley: New York, 1983.