journal article·2009-07-28

Deciphering the Structural Properties That Confer Stability to a DNA Nanocage

Mattia Falconi, Francesco Oteri, Giovanni Chillemi, Felicie F. Andersen, David Tordrup, Cristiano L. P. Oliveira, Jan S. Pedersen, Birgitta R. Knudsen, Alessandro Desideri

ACS Nano· Volume 3· Issue 7
Publisher page

Abstract

A DNA nanocage has been recently characterized by small-angle X-ray scattering (SAXS) and cryo-transmission electron microscopy as a DNA octahedron having a central cavity larger than the apertures in the surrounding DNA lattice. Starting from the SAXS data, a DNA nanocage has been modeled and simulated by classical molecular dynamics to evaluate in silico its structural properties and stability. Global properties, principal component analysis, and DNA geometrical parameters, calculated along the entire trajectory, indicate that the cage is stable and that the B-DNA conformation, also if slightly distorted, is maintained for all the simulation time. Starting from the initial model, the nanocage scaffold undergoes a contraction of the thymidine strands, connecting the DNA double helices, suggesting that the length of the thymidine strands is a crucial aspect in the modulation of the nanocage stability. A comparison of the average structure as obtained from the simulation shows good agreement with the SAXS experimental data.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Advanced biosensing and bioanalysis techniques · DNA and Nucleic Acid Chemistry · RNA Interference and Gene Delivery

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

Affiliations

Department of Biology and Center of Biostatistics and Bioinformatics, University of Rome “Tor Vergata”, Via della Ricerca Scientifica 1, 00133 Rome, Italy

NAST Nanoscience & Nanotechnology & Innovative Instrumentation, University of Rome “Tor Vergata”, Via della Ricerca Scientifica 1, 00133 Rome, Italy

CASPUR Inter-University Consortium for the Application of Super-Computing for Universities and Research, Via dei Tizii 6, Rome 00185, Italy

Department of Molecular Biology and Interdisciplinary Nanoscience Center (iNANO), Aarhus University, C.F. Møllers Allé, Bldg. 130, 8000 Aarhus C, Denmark

Department of Chemistry and Interdisciplinary Nanoscience Center (iNANO), Aarhus University, Langelandsgade 140, 8000 Aarhus C, Denmark

References (45)

Show source-provided references
1. Seeman N. C. · Annu. Rev. Biophys. Biomol. Struct. · 1998 · 27 · 22510.1146/annurev.biophys.27.1.225 ↗
2. Seeman N. C. · Nature · 2003 · 421 · 42710.1038/nature01406 ↗
3. Seeman N. C. · Q. Rev. Biophys. · 2005 · 38 · 36310.1017/S0033583505004087 ↗
4. Seeman N. C. · Trends Biochem. Sci. · 2005 · 30 · 11910.1016/j.tibs.2005.01.007 ↗
5. Ding B. · Science · 2006 · 314 · 158310.1126/science.1131372 ↗
6. Andersen F. F. · J. Mol. Biol. · 2003 · 330 · 23510.1016/S0022-2836(03)00593-X ↗
7. Liao S. · Biochemistry · 2004 · 43 · 152010.1021/bi0358061 ↗
8. Lee J. · Genes Dev. · 1997 · 11 · 306110.1101/gad.11.22.3061 ↗
9. Winfree E. · Nature · 1998 · 394 · 53910.1038/28998 ↗
10. Yan H. · Science · 2003 · 301 · 188210.1126/science.1089389 ↗
11. Malo J. · Angew. Chem., Int. Ed. · 2005 · 44 · 305710.1002/anie.200463027 ↗
12. Rinker S. · Chem. Commun. · 2006 · 25 · 267510.1039/b603872g ↗
13. Rothemund P. W. K. · Nature · 2006 · 440 · 29710.1038/nature04586 ↗
14. Chen J. H. · Nature · 1991 · 350 · 63110.1038/350631a0 ↗
15. Zhang Y. · J. Am. Chem. Soc. · 1994 · 116 · 166110.1021/ja00084a006 ↗
16. Shih W. M. · Nature · 2004 · 427 · 61810.1038/nature02307 ↗
17. Goodman R. P. · Science · 2005 · 310 · 166110.1126/science.1120367 ↗
18. Erben C. M. · J. Am. Chem. Soc. · 2007 · 6 · 699210.1021/ja071493b ↗
19. Aldaye F. A. · J. Am. Chem. Soc. · 2007 · 129 · 1337610.1021/ja075966q ↗
20. Andersen F. F. · Nucleic Acids Res. · 2008 · 36 · 111310.1093/nar/gkm1124 ↗
21. Maiti P. K. · Nucleic Acids Res. · 2004 · 32 · 604710.1093/nar/gkh931 ↗
22. Maiti P. K. · Biophys. J. · 2006 · 90 · 146310.1529/biophysj.105.064733 ↗
23. Maiti P. K. · J. Nanosci. Nanotechnol. · 2007 · 7 · 171210.1166/jnn.2007.704 ↗
24. Lankas F. · Structure · 2006 · 14 · 152710.1016/j.str.2006.08.004 ↗
25. Harris S. A. · Nucleic Acids Res. · 2007 · 36 · 2110.1093/nar/gkm891 ↗
26. Garcia A. E. · Phys. Rev. Lett. · 1992 · 68 · 269610.1103/PhysRevLett.68.2696 ↗
27. Falconi M. · Biophys. J. · 2008 · 95 · 110810.1529/biophysj.108.130849 ↗
28. Chillemi G. · Biophys. J. · 1997 · 73 · 100710.1016/S0006-3495(97)78134-7 ↗
29. Arcangeli C. · Biophys. Chem. · 2001 · 90 · 4510.1016/S0301-4622(01)00128-4 ↗
30. Hess B. · Phys. Rew. E · 2002 · 65 · 3191010.1103/PhysRevE.65.031910 ↗
31. McCammon J. A. · 1987 · 7910.1017/CBO9781139167864.006 ↗
32. Case D. A. · J. Comput. Chem. · 2005 · 26 · 166810.1002/jcc.20290 ↗
33. Duan Y. · J. Comput. Chem. · 2003 · 24 · 199910.1002/jcc.10349 ↗
34. Ponder J. W. · Adv. Protein Chem. · 2003 · 66 · 2710.1016/S0065-3233(03)66002-X ↗
35. Jorgensen W. L. · J. Chem. Phys. · 1983 · 79 · 92610.1063/1.445869 ↗
36. Berendsen H. J. C. · J. Comput. Phys. · 1984 · 81 · 3684
37. Darden T. · J. Chem. Phys. · 1993 · 98 · 1008910.1063/1.464397 ↗
38. Cheatham T. E. · J. Am. Chem. Soc. · 1995 · 117 · 419310.1021/ja00119a045 ↗
39. Ryckaert J. P. · J. Comput. Phys. · 1977 · 23 · 32710.1016/0021-9991(77)90098-5 ↗
40. Hess B. · J. Chem. Theory Comput. · 2008 · 4 · 43510.1021/ct700301q ↗
41. Lavery R. · J. Biomol. Struct. Dyn. · 1989 · 6 · 65510.1080/07391102.1989.10507728 ↗
42. Hubbard S. J. · 1993
43. Pedersen J. S. · J. Appl. Crystallogr. · 2004 · 37 · 36910.1107/S0021889804004170 ↗
44. Pedersen J. S. · Adv. Colloid Interface Sci. · 1997 · 70 · 17110.1016/S0001-8686(97)00312-6 ↗
45. Humphrey W. · J. Mol. Graph. · 1996 · 14 · 3310.1016/0263-7855(96)00018-5 ↗