Formation mechanism of chalcogenide nanocrystals confined inside genetically engineered virus-like particles

Scientific Reports

Volumn 4, Issue , 2014, Pages

  Zhou, Ziyou ^a,b   Bedwell, Gregory J ^c   Li, Rui ^c   Prevelige, Peter E ^c   Gupta, Arunava ^a,b  

^a University of Alabama   (United States)

^b University of Alabama   (United States)

^c University of Alabama at Birmingham   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CADMIUM DERIVATIVE; CAPSID PROTEIN; CHALCOGEN; NANOPARTICLE;

CATALYSIS; CHEMISTRY; ENTEROBACTERIA PHAGE P22; GENETIC ENGINEERING; GENETICS; HUMAN; MATERIALS TESTING; VIRION;

BACTERIOPHAGE P22; CADMIUM COMPOUNDS; CAPSID PROTEINS; CATALYSIS; CHALCOGENS; GENETIC ENGINEERING; HUMANS; MATERIALS TESTING; NANOPARTICLES; VIRION;

EID: 84908087356     PISSN: None     EISSN: 20452322     Source Type: Journal    
DOI: 10.1038/srep03832     Document Type: Article

References (60)

1. Douglas, T. & Young, M. Viruses: Making friends with old foes. Science 312, 873-875 (2006).
2. Douglas, T. & Young, M. Host-guest encapsulation of materials by assembled virus protein cages. Nature 393, 152-155 (1998).
3. Steinmetz, N. F. et al. Site-specific and spatially controlled addressability of a new viral nanobuilding block: sulfolobus islandicus rod-shaped virus 2. Adv. Funct. Mater. 18, 3478-3486 (2008).
4. Li, F. & Wang, Q. Fabrication of nanoarchitectures templated by virus-based nanoparticles: strategies and applications. Small DOI: 10.1002/smll.201301393.
5. Zahr, O. K. & Blum, A. S. Solution phase gold nanorings on a viral protein template. Nano Lett. 12, 629-633 (2012).
6. Brasch, M. et al. Encapsulation of phthalocyanine supramolecular stacks into virus-like particles. J. Am. Chem. Soc. 133, 6878-6881 (2011).
7. Li, F. et al. Tunable, discrete, three-dimensional hybrid nanoarchitectures. Angew. Chem. Int. Ed. 50, 4202-4205 (2011).
8. Li, F. et al. Monofunctionalization of protein nanocages. J. Am. Chem. Soc. 133, 20040-20042 (2011).
9. Lucon, J. et al.Use of the interior cavity of the P22 capsid for site-specific initiation of atom-transfer radical polymerization with high-density cargo loading. Nat. Chem. 4, 781-788 (2012).
10. Nam, K. T., Peelle, B. R., Lee, S. W.&Belcher, A. M. Genetically driven assembly of nanorings based on the M13 virus. Nano Lett. 4, 23-27 (2004).
11. Martinez-Morales, A. A. et al. Synthesis and characterization of iron oxide derivatized mutant cowpea mosaic virus hybrid nanoparticles. Adv. Mater. 20, 4816-4820 (2008).
12. Li, F. et al. Three-dimensional gold nanoparticle clusters with tunable cores templated by a viral protein scaffold. Small 8, 3832-3838 (2012).
13. Lewis, J. D. et al. Viral nanoparticles as tools for intravital vascular imaging. Nat. Med. 12, 354-360 (2006).
14. Lee, L. A., Niu, Z. W. & Wang, Q. Viruses and virus-like protein assemblieschemically programmable nanoscale building blocks. Nano Res. 2, 349-364 (2009).
15. Dixit, S. K. et al. Quantum dot encapsulation in viral capsids. Nano Lett. 6, 1993-1999 (2006).
16. Brunel, F. M. et al. Hydrazone ligation strategy to assemble multifunctional viral nanoparticles for cell imaging and tumor targeting. Nano Lett. 10, 1093-1097 (2010).
17. Patterson, D. P., Prevelige, P. E. & Douglas, T. Nanoreactors by programmed enzyme encapsulation inside the capsid of the bacteriophage P22. Acs Nano 6, 5000-5009 (2012).
18. Shen, L., Bao, N., Zhou, Z., Prevelige, P. E. & Gupta, A. Materials design using genetically engineered proteins. J. Mater. Chem. 21, 18868-18876 (2011).
19. Li, F. et al. Insights into stabilization of a viral protein cage in templating complex nanoarchitectures: roles of disulfide bonds. Small DOI: 10.1002/smll.201300860.
20. Wang, Q., Lin, T., Tang, L., Johnson, J. E. & Finn,M. G. Icosahedral virus particles as addressable nanoscale building blocks. Angew. Chem. Int. Edit. 41, 459-462 (2002).
21. Capehart, S. L., Coyle, M. P., Glasgow, J. E.&Francis, M. B. Controlled integration of gold nanoparticles and organic fluorophores using synthetically modified MS2 viral capsids. J. Am. Chem. Soc. 135, 3011-3016 (2013).
22. Kale, A., Bao, Y., Zhou, Z., Prevelige, P. E. & Gupta, A. Directed self-assembly of CdS quantum dots on bacteriophage P22 coat protein templates. Nanotechnology 24, 045603 (2013).
23. Glasgow, J. E., Capehart, S. L., Francis, M. B. & Tullman-Ercek, D. Osmolytemediated encapsulation of proteins inside MS2 viral capsids. ACS Nano 6, 8658-8664 (2012).
24. Dujardin, E., Peet, C., Stubbs, G., Culver, J. N. &Mann, S. Organization ofmetallic nanoparticles using tobacco mosaic virus templates. Nano Lett. 3, 413-417 (2003).
25. Stephanopoulos, N. et al. Immobilization and one-dimensional arrangement of virus capsids with nanoscale precision using DNA origami. Nano Lett. 10, 2714-2720 (2010).
26. Qazi, S. et al. P22 viral capsids as nanocomposite high-relaxivity MRI contrast agents. Mol. Pharmaceut 10, 11-17 (2013).
27. Kang, S., Uchida, M., O'Neil, A., Li, R., Prevelige, P. E. & Douglas, T. Implementation of P22 viral capsids as nanoplatforms. Biomacromolecules 11, 2804-2809 (2010).
28. Shen, L., Bao, N., Prevelige, P. E. & Gupta, A. Fabrication of ordered nanostructures of sulfide nanocrystal assemblies over self-assembled genetically engineered P22 coat protein. J. Am. Chem. Soc. 132, 17354-17357 (2010).
29. Parker, M. H. & Prevelige, P. E. Electrostatic interactions drive scaffolding/coat protein binding and procapsid maturation in bacteriophage P22. Virology 250, 337-349 (1998).
30. Mao, C. et al.Viral assembly of oriented quantum dot nanowires. Proc. Natl. Acad. Sci. U. S. A. 100, 6946-6951 (2003).
31. Mao, C. et al. Virus-based toolkit for the directed synthesis of magnetic and semiconducting nanowires. Science 303, 213-217 (2004).
32. Prevelige, P. E., Thomas, D. & King, J. Scaffolding protein regulates the polymerization of P22 coat subunits into icosahedral shells in vitro. J. Mol. Biol. 202, 743-757 (1988).
33. Prevelige, P. E., Thomas, D. & King, J. Nucleation and growth phases in the polymerization of coat and scaffolding subunits into icosahedral procapsid shells. Biophys. J. 64, 824-835 (1993).
34. Reichhardt, C., Uchida, M., O'Neil, A., Li, R., Prevelige, P. E. & Douglas, T. Templated assembly of organic-inorganic materials using the core shell structure of the P22 bacteriophage. Chem. Commun. 47, 6326-6328 (2011).
35. Flynn, C. E. et al. Synthesis and organization of nanoscale II-VI semiconductor materials using evolved peptide specificity and viral capsid assembly. J. Mater. Chem. 13, 2414-2421 (2003).
36. Tuma, R. et al. A helical coat protein recognition domain of the bacteriophage P22 scaffolding protein. J. Mol. Biol. 281, 81-94 (1998).
37. Parker, M. H., Jablonsky, M., Casjens, S., Sampson, L., Krishna, N. R. & Prevelige, P. E. Cloning, purification, and preliminary characterization by circular dichroism and NMR of a carboxyl-terminal domain of the bacteriophage P22 scaffolding protein. Protein Sci. 6, 1583-1586 (1997).
38. Bao, N., Shen, L., Takata, T. & Domen, K. Self-templated synthesis of nanoporous CdS nanostructures for highly efficient photocatalytic hydrogen production under visible light. Chem. Mater. 20, 110-117 (2008).
39. Bao, N., Shen, L., Lu, X., Yanagisawa, K. & Feng, X. Room-temperature syntheses of CdS nanocrystals templated by triblock copolymer in aqueous solution under air condition. Chem. Phys. Lett. 377, 119-124 (2003).
40. Parker, M. H., Brouillette, C. G. & Prevelige, P. E. Kinetic and calorimetric evidence for two distinct scaffolding protein binding populations within the bacteriophage P22 procapsid. Biochemistry 40, 8962-8970 (2001).
41. Padilla-Meier, G. P. & Teschke, C. M. Conformational changes in bacteriophage P22 scaffolding protein induced by interaction with coat protein. J. Mol. Biol. 410, 226-240 (2011).
42. Gebauer, D., Voelkel, A. & Coelfen, H. Stable prenucleation calcium carbonate clusters. Science 322, 1819-1822 (2008).
43. Pouget, E. M., Bomans, P. H. H., Dey, A., Frederik, P. M., de With, G. & Sommerdijk, N. A. J. M. The development of morphology and structure in hxagonal vaterite. J. Am. Chem. Soc. 132, 11560-11565 (2010).
44. Pouget, E. M., Bomans, P. H. H., Goos, J. A. C. M., Frederik, P. M., deWith, G. & Sommerdijk, N. A. J. M. The initial stages of template-controlled CaCO3 formation revealed by Cryo-TEM. Science 323, 1455-1458 (2009).
45. Dey, A. et al. The role of prenucleation clusters in surface-induced calcium phosphate crystallization. Nat. Mater. 9, 1010-1014 (2010).
46. Gebauer, D. & Coelfen, H. Prenucleation clusters and non-classical nucleation. Nano Today 6, 564-584 (2011).
47. Karan, S. & Maw, B. Tunable visible-light emission from CdS nanocrystallites prepared under microwave irradiation. J. Phys. Chem. C 111, 16734-16741 (2007).
48. Henglein, A. Small-particle research: physicochemical properties of extremely small colloidal metal and semicondutor particles. Chem. Rev. 89, 1861-1873 (1989).
49. Torimoto, T. et al. Characterization of ultrasmall CdS nanoparticles prepared by the size-selective photoetching technique. J. Phys. Chem. B 105, 6838-6845 (2001).
50. Miyake, M., Torimoto, T., Sakata, T., Mori, H. & Yoneyama, H. Photoelectrochemical characterization of nearly monodisperse CdS nanoparticles-immobilized gold electrodes. Langmuir 15, 1503-1507 (1999).
51. Yu,W., Qu, L., Guo, W. & Peng, X. Experimental determination of the extinction coefficient of CdTe, CdSe, and CdS nanocrystals. Chem. Mat. 15, 2854-2860 (2003).
52. Sugimoto, T., Dirige, G. E. & Muramatsu, A. Formation mechanism of uniform CdS particles from condensed Cd(OH)2 suspension. J. Colloid Interface Sci. 176, 442-453 (1995).
53. Sugimoto, T., Chen, S. & Muramatsu, A. Synthesis of uniform particles of CdS, ZnS, PbS and CuS from concentrated solutions of the metal chelates. Colloid Surf. A-Physicochem. Eng. Asp. 135, 207-226 (1998).
54. Kubota, N. & Mullin, J. W. A kinetic model for crystal growth from aqueous solution in the presence of impurity. J. Cryst. Growth 152, 203-208 (1995).
55. Rieger, J., Frechen, T.,Cox, G.,Heckmann, W., Schmidt, C.&Thieme, J. Precursor structures in the crystallization/precipitation processes of CaCO3 and control of particle formation by polyelectrolytes. Faraday Discuss. 136, 265-277 (2007).
56. Amjad, Z. Kinetic study of the seeded growth of calcium carbonate in the presence of benzenepolycarboxylic acids. Langmuir 3, 224-228 (1987).
57. Njegic-Dzakula, B., Brecevic, L., Falini, G. & Kralj, D. Calcite crystal growth kinetics in the presence of charged synthetic polypeptides. Cryst. Growth Des. 9, 2425-2434 (2009).
58. Shen, L., Bao, N., Prevelige, P. E. & Gupta, A. Escherichia coli bacteria-templated synthesis of nanoporous cadmium sulfide hollow microrods for efficient photocatalytic hydrogen production. J. Phys. Chem. C 114, 2551-2559 (2010).
59. Ma, N., Yang, J., Stewart, K. M. & Kelley, S. O. DNA-passivated CdS nanocrystals: luminescence, bioimaging, and toxicity profiles. Langmuir 23, 12783-12787 (2007).
60. Santra, S., Yang, H., Holloway, P. H., Stanley, J. T. & Mericle, R. A. Synthesis of water-dispersible fluorescent, radio-opaque, and paramagnetic CdS: Mn/ZnS quantum dots: A multifunctional probe for bioimaging. J. Am. Chem. Soc. 127, 1656-1657 (2005).