Supramolecular chirality and crystallization from biocatalytic self-assembly in lipidic cubic mesophases
Source abstract
Abstract
Biocatalytic self-assembly in a nanoconfined environment is widely used in nature to construct complex structures that endow special characteristics to life. There is tremendous interest in mimicking such bottom-up processes to fabricate functional materials. In this study, we have investigated a novel biomimetic scaffold based on lipidic cubic mesophases (LCMs), which provide a special nanoconfined environment for biocatalytic self-assembly and subsequent formation of organic crystals. (R)-Benzoin generated in situ from benzaldehyde in a reaction catalyzed by the enzyme benzaldehyde lyase (BAL) exhibits - when confined within LCMs - enhanced chirality compared to (R)-benzoin in solution or (R)-benzoin-doped LCMs. We infer that a metastable state is formed under kinetic control that displays enhanced supramolecular chirality. As they age, these metastable structures can further grow into thermodynamically stable crystals. The biomimetic, nanoconfined environment provided by the LCMs plays a key role in the development of supramolecular chirality and subsequent crystallization.
Source: openalex_inverted_index · Quality: candidate unverified · Source record ↗
Research context
OpenAlex topics: Supramolecular Self-Assembly in Materials · Lipid Membrane Structure and Behavior · Glycosylation and Glycoproteins Research
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Health Science and Technology
ETH Zurich
8092 Zürich
Switzerland
Department of Chemistry
University of Zurich
8057 Zurich
Department of Materials
Funding
China Scholarship Council · Eidgenössische Technische Hochschule Zürich
References (44)
Show source-provided references
1. H. Lodish , A.Berk , P.Matsudaira , C. A.Kaiser , M.Krieger , M. P.Scott , S. L.Zipursky and J.Darnell , Molecular Cell Biology , Freeman , New York , 5th edn, 2003
2. Yang · Acc. Chem. Res. · 2008 · 41 · 31510.1021/ar7001914 ↗
3. Kuchler · Nat. Nanotechnol. · 2016 · 11 · 40910.1038/nnano.2016.54 ↗
4. B. Alberts , A.Johnson , J.Lewis , M.Raff , K.Roberts and P.Walter , Molecular Biology of the Cell , Garland Science , New York , 2002
5. Conrado · Curr. Opin. Biotechnol. · 2008 · 19 · 49210.1016/j.copbio.2008.07.006 ↗
6. Williams · Nat. Nanotechnol. · 2009 · 4 · 1910.1038/nnano.2008.378 ↗
7. Vigier-Carrière · Angew. Chem., Int. Ed. · 2015 · 54 · 1019810.1002/anie.201504761 ↗
8. Vigier-Carrière · Langmuir · 2017 · 33 · 826710.1021/acs.langmuir.7b01532 ↗
9. Hirst · Nat. Chem. · 2010 · 2 · 108910.1038/nchem.861 ↗
10. Um · Nat. Mater. · 2006 · 5 · 79710.1038/nmat1741 ↗
11. Liu · Bioconjugate Chem. · 2018 · 29 · 180910.1021/acs.bioconjchem.8b00197 ↗
12. Conte · ACS Appl. Mater. Interfaces · 2017 · 9 · 326610.1021/acsami.6b13162 ↗
13. Conte · ACS Appl. Mater. Interfaces · 2018 · 10 · 306910.1021/acsami.7b15456 ↗
14. Kalafatovic · Biomaterials · 2016 · 98 · 19210.1016/j.biomaterials.2016.04.039 ↗
15. Feng · J. Am. Chem. Soc. · 2017 · 139 · 395010.1021/jacs.7b00070 ↗
16. Wang · J. Am. Chem. Soc. · 2016 · 138 · 1075810.1021/jacs.6b06075 ↗
17. Kuang · Angew. Chem., Int. Ed. · 2014 · 53 · 810410.1002/anie.201402216 ↗
18. Zhou · Chem. · 2016 · 1 · 24610.1016/j.chempr.2016.07.003 ↗
19. Pires · J. Am. Chem. Soc. · 2015 · 137 · 57610.1021/ja5111893 ↗
20. Yang · Angew. Chem., Int. Ed. · 2007 · 46 · 821610.1002/anie.200701697 ↗
21. Kuang · Angew. Chem., Int. Ed. · 2013 · 52 · 694410.1002/anie.201302658 ↗
22. Zhou · J. Am. Chem. Soc. · 2015 · 137 · 1004010.1021/jacs.5b06181 ↗
23. Gao · Nat. Commun. · 2012 · 3 · 103310.1038/ncomms2040 ↗
24. Li · Adv. Healthcare Mater. · 2017 · 6 · 160140010.1002/adhm.201601400 ↗
25. N. Garti , P.Somasndaran and R.Mezzenga , Self-assembled Supermolecular Architectures: Lyotropic Liquid Crystals , A John Wiley & Sons Inc. , New York, America , 2012 , pp. 1–2010.1002/9781118336632 ↗
26. Li · Proc. Natl. Acad. Sci. U. S. A. · 2011 · 108 · 863910.1073/pnas.1101815108 ↗
27. Nazaruk · J. Colloid Interface Sci. · 2012 · 385 · 13010.1016/j.jcis.2012.06.087 ↗
28. Fong · J. Controlled Release · 2009 · 135 · 21810.1016/j.jconrel.2009.01.009 ↗
29. Zhou · ACS Catal. · 2018 · 7 · 581010.1021/acscatal.8b01716 ↗
30. Vallooran · Adv. Funct. Mater. · 2016 · 26 · 18110.1002/adfm.201503428 ↗
31. Sun · Nanoscale · 2014 · 6 · 685310.1039/C4NR01394H ↗
32. Sun · Langmuir · 2015 · 31 · 455810.1021/acs.langmuir.5b00579 ↗
33. Sun · J. Phys. Chem. Lett. · 2016 · 7 · 150710.1021/acs.jpclett.6b00416 ↗
34. Demir · Adv. Synth. Catal. · 2002 · 344 · 9610.1002/1615-4169(200201)344:1<96::AID-ADSC96>3.0.CO;2-Z ↗
35. Shanmuganathan · Green Chem. · 2010 · 12 · 224010.1039/c0gc00590h ↗
36. L. H. Keith and D. B.Walters , National Toxicology Program's Chemical Solubility Compendium , Taylor and Francis , 1991 , p. 51
37. Bredehöft · Chirality · 2014 · 26 · 37310.1002/chir.22329 ↗
38. Zsila · Org. Biomol. Chem. · 2004 · 2 · 290210.1039/B409724F ↗
39. Adams · Soft Matter · 2010 · 6 · 414410.1039/c0sm00409j ↗
40. Mondal · Langmuir · 2016 · 32 · 537310.1021/acs.langmuir.6b01053 ↗
41. Wang · Chem. Soc. Rev. · 2016 · 45 · 558910.1039/C6CS00176A ↗
42. Zhu · Chem. – Eur. J. · 2010 · 16 · 317610.1002/chem.200902139 ↗
43. Wang · Cryst. Growth Des. · 2008 · 8 · 88410.1021/cg070619d ↗
44. Adamcik · Angew. Chem., Int. Ed. · 2018 · 57 · 837010.1002/anie.201713416 ↗