journal article·2011-02-22

Protein-Directed Assembly of Arbitrary Three-Dimensional Nanoporous Silica Architectures

Constantine Y. Khripin, Denis Pristinski, Darren R. Dunphy, C. Jeffrey Brinker, Bryan Kaehr

ACS Nano· Volume 5· Issue 2
Publisher page

Abstract

Through precise control of nanoscale building blocks, such as proteins and polyamines, silica condensing microorganisms are able to create intricate mineral structures displaying hierarchical features from nano- to millimeter-length scales. The creation of artificial structures of similar characteristics is facilitated through biomimetic approaches, for instance, by first creating a bioscaffold comprised of silica condensing moieties which, in turn, govern silica deposition into three-dimensional (3D) structures. In this work, we demonstrate a protein-directed approach to template silica into true arbitrary 3D architectures by employing cross-linked protein hydrogels to controllably direct silica condensation. Protein hydrogels are fabricated using multiphoton lithography, which enables user-defined control over template features in three dimensions. Silica deposition, under acidic conditions, proceeds throughout protein hydrogel templates via flocculation of silica nanoparticles by protein molecules, as indicated by dynamic light scattering (DLS) and time-dependent measurements of elastic modulus. Following silica deposition, the protein template can be removed using mild thermal processing yielding high surface area (625 m(2)/g) porous silica replicas that do not undergo significant volume change compared to the starting template. We demonstrate the capabilities of this approach to create bioinspired silica microstructures displaying hierarchical features over broad length scales and the infiltration/functionalization capabilities of the nanoporous silica matrix by laser printing a 3D gold image within a 3D silica matrix. This work provides a foundation to potentially understand and mimic biogenic silica condensation under the constraints of user-defined biotemplates and further should enable a wide range of complex inorganic architectures to be explored using silica transformational chemistries, for instance silica to silicon, as demonstrated herein.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Diatoms and Algae Research · Protist diversity and phylogeny · Photonic Crystals and Applications

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

Affiliations

NSF/UNM Center for Micro-Engineered Materials, Departments of Chemical and Nuclear Engineering and Molecular Genetics and Microbiology, University of New Mexico, Albuquerque, New Mexico, United States

Polymers Division, National Institute of Standards and Technology, Gaithersburg, Maryland, United States

Advanced Materials Laboratory, Sandia National Laboratories, Albuquerque, New Mexico, United States

References (53)

Show source-provided references
1. Hildebrand M. · Chem. Rev. · 2008 · 108 · 485510.1021/cr078253z ↗
2. Dickerson M. B. · Chem. Rev. · 2008 · 108 · 493510.1021/cr8002328 ↗
3. Gordon R. · Trends Biotechnol. · 2009 · 27 · 11610.1016/j.tibtech.2008.11.003 ↗
4. Losic D. · Adv. Mater. · 2009 · 21 · 294710.1002/adma.200803778 ↗
5. Parker A. R. · Nat. Nanotech. · 2007 · 2 · 34710.1038/nnano.2007.152 ↗
6. Sanchez C. · Nat. Mater. · 2005 · 4 · 27710.1038/nmat1339 ↗
7. Cha J. N. · Proc. Natl. Acad. Sci. U.S.A. · 1999 · 96 · 36110.1073/pnas.96.2.361 ↗
8. Luckarift H. R. · Nat. Biotechnol. · 2004 · 22 · 21110.1038/nbt931 ↗
9. Kroger N. · Science · 2002 · 298 · 58410.1126/science.1076221 ↗
10. Groeger C. · Cell Biochem. Biophys. · 2008 · 50 · 2310.1007/s12013-007-9003-2 ↗
11. Losic D. · New J. Chem. · 2006 · 30 · 90810.1039/b600073h ↗
12. Losic D. · Adv. Funct. Mater. · 2007 · 17 · 243910.1002/adfm.200600872 ↗
13. Shian S. · J. Am. Chem. Soc. · 2005 · 89 · 694
14. Cai Y. · J. Am. Chem. Soc. · 2005 · 88 · 2005
15. Unocic R. R. · Chem. Commun. · 2004 · 2004 · 79610.1039/b400599f ↗
16. Sandhage K. H. · Adv. Mater. · 2002 · 14 · 42910.1002/1521-4095(20020318)14:6<429::AID-ADMA429>3.0.CO;2-C ↗
17. Zhao J. · J. Mater. Res. · 2005 · 20 · 28210.1557/JMR.2005.0046 ↗
18. Bao Z. · Nature · 2007 · 446 · 17210.1038/nature05570 ↗
19. Gaddis C. S. · J. Mater. Res. · 2004 · 19 · 254210.1557/JMR.2004.0342 ↗
20. Li X. · Appl. Surf. Sci. · 2003 · 207 · 37810.1016/S0169-4332(03)00010-2 ↗
21. Cai X. · Eur. J. Inorg. Chem. · 2006 · 2006 · 364110.1002/ejic.200600339 ↗
22. Holmes S. M. · Chem. Commun. · 2006 · 2006 · 266210.1039/b600708b ↗
23. Rosi N. L. · Angew. Chem. · 2004 · 116 · 561610.1002/ange.200460905 ↗
24. Payne E. K. · Angew. Chem. · 2005 · 117 · 519210.1002/ange.200500988 ↗
25. Zhou H. · Eur. J. Inorg. Chem. · 2008 · 2009 · 21110.1002/ejic.200800764 ↗
26. Ford J. · Chem. Mater. · 2007 · 19 · 557010.1021/cm071566q ↗
27. Moon J. H. · J. Mater. Chem. · 2009 · 19 · 468710.1039/b901226e ↗
28. Xu M. · Soft Matter · 2006 · 2 · 20510.1039/b517278k ↗
29. LaFratta C. N. · Angew. Chem., Int. Ed. · 2007 · 46 · 623810.1002/anie.200603995 ↗
30. Tétreault N. · Adv. Mater. · 2006 · 18 · 45710.1002/adma.200501674 ↗
31. Kroger N. · Science · 1999 · 286 · 112910.1126/science.286.5442.1129 ↗
32. Morse D. E. · Trends Biotechnol. · 1999 · 17 · 23010.1016/S0167-7799(99)01309-8 ↗
33. Coradin T. · Colloids Surf., B · 2003 · 29 · 18910.1016/S0927-7765(02)00208-4 ↗
34. Luckarift H. · Colloids Surf., B · 2007 · 58 · 2810.1016/j.colsurfb.2006.08.013 ↗
35. Gautier C. · Colloids Surf., B · 2008 · 65 · 14010.1016/j.colsurfb.2008.03.005 ↗
36. Bassindale A. · J. Mater. Chem. · 2009 · 19 · 760610.1039/b916412j ↗
37. Brott L. L. · Nature · 2001 · 413 · 29110.1038/35095031 ↗
38. Kaehr B. · J. Am. Chem. Soc. · 2007 · 129 · 190410.1021/ja068390y ↗
39. Nielson R. · Small · 2009 · 5 · 12010.1002/smll.200801084 ↗
40. Kaehr B. · Proc. Natl. Acad. Sci. U.S.A. · 2004 · 101 · 1610410.1073/pnas.0407204101 ↗
41. Khripin C. Y. · Soft Matter · 2010 · 6 · 284210.1039/c001193b ↗
42. Kaehr B. · Proc. Natl. Acad. Sci. U.S.A. · 2008 · 105 · 885010.1073/pnas.0709571105 ↗
43. Iler R. K. · 1979
44. Kaehr B. · Lab Chip · 2009 · 9 · 263210.1039/b908119d ↗
45. Connell J. · mBio · 2010 · 1 · e00202−1010.1128/mBio.00202-10 ↗
46. Carter D. · Advances in protein chemistry · 1994 · 45 · 15310.1016/S0065-3233(08)60640-3 ↗
47. Bergmann N. · Prog. Polym. Sci. · 2008 · 33 · 27110.1016/j.progpolymsci.2007.09.004 ↗
48. Tanaka T. · IEEE Trans. Magn. · 2007 · 43 · 82810.1109/TMAG.2006.888445 ↗
49. Royon A. · Adv. Mater. · 2010 · 22 · 528210.1002/adma.201002413 ↗
50. Wu P. · Adv. Mater. · 2000 · 12 · 143810.1002/1521-4095(200010)12:19<1438::AID-ADMA1438>3.0.CO;2-Y ↗
51. Meisel D. · Adv. Mater. · 2006 · 18 · 296410.1002/adma.200600412 ↗
52. Fancy D. · Proc. Natl. Acad. Sci. U.S.A. · 1999 · 96 · 602010.1073/pnas.96.11.6020 ↗
53. Yamasaki M. · Int. J. Biol. Macromol. · 1990 · 12 · 26310.1016/0141-8130(90)90007-W ↗