Symbiotic assembly of peptide nano-mosaics at solid interfaces
Source abstract
Abstract
The spontaneous co-organization of distinct biomolecules at interfaces enables many of Nature's hierarchical organizations involving both hard and soft materials. Engineering efforts to mimic such hybrid complexes rely on our ability to rationally structure biomolecules at inorganic interfaces. Control over the nanoscale structure of patterned biomolecules remains challenging due to difficulties in controlling the multifarious interactions involved. This work discusses binary peptide assembly as a means to fabricate biomolecular nano-mosaics at graphite surfaces with predictable structures. Distinct peptide-substrate interactions lead to divergent crystallographic growth directions, molecular scale immiscibility, and a symbiotic assembly phenomenon. We present a symbiotic assembly model that accurately predicts the binary assembly structure relying solely on the constituent peptide nucleation kinetics and molar fractions. The ability to tune such biomolecular nano-mosaic structures facilitates the bottom up fabrication of high-density, multifunctional interfaces for nanotechnology.
Source: openalex_inverted_index · Quality: candidate unverified · Source record ↗
Research context
OpenAlex topics: Supramolecular Self-Assembly in Materials · Diatoms and Algae Research · Advanced biosensing and bioanalysis techniques
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Molecular Engineering and Sciences Institute
University of Washington
Seattle
USA
Department of Material Science and Engineering
Department of Chemical Engineering
Funding
Division of Materials Research
References (48)
Show source-provided references
1. Winkel · Annu. Rev. Plant Biol. · 2004 · 55 · 8510.1146/annurev.arplant.55.031903.141714 ↗
2. Suss · Proc. Natl. Acad. Sci. U. S. A. · 1993 · 90 · 551410.1073/pnas.90.12.5514 ↗
3. Castellana · Nat. Biotechnol. · 2014 · 32 · 101110.1038/nbt.3018 ↗
4. Wheeldon · Nat. Chem. · 2016 · 8 · 29910.1038/nchem.2459 ↗
5. Bang · ACS Nano · 2009 · 3 · 146710.1021/nn900324q ↗
6. Song · Nano Lett. · 2005 · 5 · 155710.1021/nl050813r ↗
7. Wang · J. Am. Chem. Soc. · 2008 · 130 · 948110.1021/ja801931m ↗
8. Conrado · Curr. Opin. Biotechnol. · 2008 · 19 · 49210.1016/j.copbio.2008.07.006 ↗
9. Jia · Biotechnol. Bioeng. · 2014 · 111 · 20910.1002/bit.25136 ↗
10. Dueber · Nat. Biotechnol. · 2009 · 27 · 75310.1038/nbt.1557 ↗
11. Nguyen · Adv. Mater. · 2018 · 30 · 170484710.1002/adma.201704847 ↗
12. Chen · ACS Synth. Biol. · 2015 · 4 · 810.1021/sb500113b ↗
13. Pham · Nanotechnology · 2010 · 21 · 46560310.1088/0957-4484/21/46/465603 ↗
14. Yin · Chem. Rev. · 2015 · 115 · 248310.1021/cr500537t ↗
15. Samanta · Chem. Soc. Rev. · 2011 · 40 · 256710.1039/c0cs00056f ↗
16. Zhang · Chem. Rev. · 2016 · 116 · 21510.1021/acs.chemrev.5b00608 ↗
17. Bornscheuer · Angew. Chem., Int. Ed. · 2003 · 42 · 333610.1002/anie.200301664 ↗
18. Hildebrandt · ACS Nano · 2011 · 5 · 528610.1021/nn2023123 ↗
19. Georgakilas · Chem. Rev. · 2016 · 116 · 546410.1021/acs.chemrev.5b00620 ↗
20. Talbert · Colloids Surf., B · 2012 · 93 · 810.1016/j.colsurfb.2012.01.003 ↗
21. Ganesan · J. Mater. Chem. · 2010 · 20 · 732210.1039/b926690a ↗
22. Stephanopoulos · Acta Mater. · 2013 · 61 · 91210.1016/j.actamat.2012.10.046 ↗
23. Zhang · Nat. Biotechnol. · 2003 · 21 · 117110.1038/nbt874 ↗
24. Seeman · Nat. Rev. Mater. · 2017 · 3 · 110.1038/natrevmats.2017.68 ↗
25. Fu · Nat. Nanotechnol. · 2014 · 9 · 53110.1038/nnano.2014.100 ↗
26. Ma · Nat. Mater. · 2017 · 16 · 76710.1038/nmat4891 ↗
27. Pyles · Nature · 2019 · 571 · 25110.1038/s41586-019-1361-6 ↗
28. Rapaport · J. Am. Chem. Soc. · 2000 · 122 · 1252310.1021/ja002238t ↗
29. Walsh · Bioconjugate Chem. · 2019 · 30 · 272710.1021/acs.bioconjchem.9b00593 ↗
30. Care · Trends Biotechnol. · 2015 · 33 · 25910.1016/j.tibtech.2015.02.005 ↗
31. Sarikaya · Nat. Mater. · 2003 · 2 · 57710.1038/nmat964 ↗
32. Kacar · Biotechnol. Bioeng. · 2009 · 103 · 69610.1002/bit.22282 ↗
33. Hnilova · J. Colloid Interface Sci. · 2012 · 365 · 9710.1016/j.jcis.2011.09.006 ↗
34. So · ACS Nano · 2012 · 6 · 164810.1021/nn204631x ↗
35. Chen · Science · 2018 · 362 · 113510.1126/science.aau4146 ↗
36. Jorgenson · Langmuir · 2020 · 36 · 31810.1021/acs.langmuir.9b02425 ↗
37. Jorgenson · Soft Matter · 2019 · 15 · 736010.1039/C9SM00426B ↗
38. Seki · Langmuir · 2017 · 34 · 181910.1021/acs.langmuir.7b02231 ↗
39. Li · ACS Appl. Mater. Interfaces · 2019 · 11 · 2067010.1021/acsami.9b04079 ↗
40. Sun · RSC Adv. · 2016 · 6 · 9688910.1039/C6RA21244A ↗
41. Khatayevich · Small · 2014 · 10 · 150510.1002/smll.201302188 ↗
42. Sear · J. Phys.: Condens. Matter · 2007 · 19 · 033101
43. De Yoreo · Rev. Mineral. Geochem. · 2003 · 54 · 5710.2113/0540057 ↗
44. Wang · Nanoscale · 2015 · 7 · 1534110.1039/C5NR00555H ↗
45. He · Nanoscale · 2020 · 12 · 1382210.1039/D0NR02271C ↗
46. Hughes · Nanoscale · 2018 · 10 · 30210.1039/C7NR06441A ↗
47. Li · Nanoscale · 2013 · 5 · 620710.1039/c3nr01644g ↗
48. Nečas · Open Phys. · 2012 · 10 · 18110.2478/s11534-011-0096-2 ↗