journal article·2020

A controlled nucleation and formation rate of self-assembled peptide nanofibers

Lei Lu, Devlin Morrison, Larry D. Unsworth

Nanoscale· Volume 12· Issue 15
Publisher page

Abstract

Self-assembling peptide matrixes are powerful platforms for encouraging tissue regeneration, but are usually formed within seconds and remain relatively static in both structure and function throughout their application. For the first time, we have shown that it is possible to extend the time it takes for peptide self-assembly so as to allow for the dynamic building of a self-assembled system over days, in the presence of an enzyme. Specifically, K5 and K10 sequences were conjugated, via a thrombin-specific cleavage domain NleTPR/SFL, to prevent the nanofiber formation and form stable nanoparticles composed of (RADA)4-GG-NleTPR/SFL-K5 and (RADA)4-GG-NleTPR/SFL-K10 that act as nucleation sites for reassembling. Upon introduction of thrombin, a model enzyme, this system showed an extremely slow rate of nanofiber formation in a parallel direction that is in sharp contrast to the well-known rapid assembly of (RADA)4 systems with random networks. These bioresponsive materials may provide a novel platform for utilizing long-term enzymatic profiles to form new nanofibers within an existing matrix over long therapeutic timeframes.
Source: europepmc · Quality: candidate unverified · Source record ↗

Research context

OpenAlex topics: Supramolecular Self-Assembly in Materials · Advanced biosensing and bioanalysis techniques · 2D Materials and Applications

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

Affiliations

School of Life Science and Engineering

Southwest Jiaotong University

Chengdu

China

Department of Chemical and Materials Engineering

University of Alberta

Edmonton

Canada

Funding

Canadian Network for Research and Innovation in Machining Technology, Natural Sciences and Engineering Research Council of Canada

References (37)

Show source-provided references
1. Branco · Acta Biomater. · 2009 · 5 · 81710.1016/j.actbio.2008.09.018 ↗
2. Matson · Chem. Commun. · 2012 · 48 · 2610.1039/C1CC15551B ↗
3. Gelain · Macromol. Biosci. · 2007 · 7 · 54410.1002/mabi.200700033 ↗
4. Zhang · Semin. Cancer Biol. · 2005 · 41310.1016/j.semcancer.2005.05.007 ↗
5. Wang · Soft Matter · 2008 · 4 · 238810.1039/b807155a ↗
6. Liu · Nanoscale · 2012 · 4 · 272010.1039/c2nr00001f ↗
7. Kim · Biomaterials · 2013 · 34 · 165710.1016/j.biomaterials.2012.11.008 ↗
8. Pan · Mater. Sci. Eng., C · 2013 · 33 · 333610.1016/j.msec.2013.04.019 ↗
9. Horii · PLoS One · 2007 · 2 · e19010.1371/journal.pone.0000190 ↗
10. Zou · J. Biomed. Mater. Res., Part A · 2010 · 95A · 112510.1002/jbm.a.32910 ↗
11. Zou · J. Biomed. Mater. Res., Part A · 2014 · 102 · 128610.1002/jbm.a.34804 ↗
12. Koss · Acta Biomater. · 2016 · 35 · 12710.1016/j.actbio.2016.02.001 ↗
13. Koss · J. Controlled Release · 2016 · 243 · 20410.1016/j.jconrel.2016.09.037 ↗
14. Koss · Acta Biomater. · 2016 · 44 · 210.1016/j.actbio.2016.08.026 ↗
15. Blombäck · Nature · 1978 · 275 · 50110.1038/275501a0 ↗
16. Strukova · Biochemistry · 2004 · 69 · 1067
17. Absar · J. Controlled Release · 2014 · 177 · 4210.1016/j.jconrel.2013.12.036 ↗
18. Zhang · Adv. Mater. · 2017 · 29 · 1604043.1
19. Bhat · Langmuir · 2016 · 32 · 119510.1021/acs.langmuir.5b04038 ↗
20. Argyo · Chem. – Eur. J. · 2012 · 18 · 42810.1002/chem.201102926 ↗
21. Li · Adv. Funct. Mater. · 2017 · 27 · 170393410.1002/adfm.201703934 ↗
22. Du · Mater. Horiz. · 2016 · 3 · 55610.1039/C6MH00307A ↗
23. Bar-Shavit · Ann. N. Y. Acad. Sci. · 1986 · 485 · 33510.1111/j.1749-6632.1986.tb34595.x ↗
24. Coughlin · Nature · 2000 · 407 · 25810.1038/35025229 ↗
25. Krenzlin · Int. J. Mol. Sci. · 2016 · 17 · 8410.3390/ijms17010084 ↗
26. Walker · Br. J. Anaesth. · 2002 · 88 · 84810.1093/bja/88.6.848 ↗
27. Sokolova · Thromb. Haemostasis · 2008 · 100 · 57610.1160/TH08-03-0131 ↗
28. Doron · Front. Neurol. · 2017 · 8 · 138
29. Kabiri · Biomacromolecules · 2013 · 14 · 394310.1021/bm401077b ↗
30. Whitney · Angew. Chem., Int. Ed. · 2013 · 52 · 32510.1002/anie.201205721 ↗
31. Ye · J. Pept. Sci. · 2008 · 14 · 15210.1002/psc.988 ↗
32. Chen · ACS Appl. Mater. Interfaces · 2016 · 8 · 1783310.1021/acsami.6b04939 ↗
33. Webber · Soft Matter · 2011 · 7 · 966510.1039/c1sm05610g ↗
34. Gong · ACS Appl. Mater. Interfaces · 2020 · 12 · 432310.1021/acsami.9b21296 ↗
35. Ji · Angew. Chem., Int. Ed. · 2016 · 55 · 105010.1002/anie.201506262 ↗
36. Zhao · Angew. Chem. · 2019 · 131 · 1543110.1002/ange.201908185 ↗
37. Liang · Nanoscale · 2017 · 9 · 1198710.1039/C7NR04370H ↗