journal article·2025Open access

Time-lapsed nanoscale maps of the elastic modulus of collagen during cross-linking by bimodal AFM

Clara Garcia-Sacristan, Ricardo Garcia

Nanoscale· Volume 17· Issue 27

Abstract

Collagen is the most abundant structural protein in mammals. Collagen in tissues is exposed to cross-linking processes such as glycation which might cause progressive tissue stiffening. Tissue stiffening might be considered a landmark of aging. Yet a quantitative characterization of the elastic modulus of collagen nanofibers under different cross-linking processes and stages is not available. Bimodal AFM was applied to generate time-lapsed maps of Young's modulus of type I collagen nanoribbons under two cross-linking processes associated, respectively, with the presence of ribose and glutaraldehyde in the solution. Elastic modulus maps were acquired for different incubation times (0, 30 min, 12 h, 24 h and 1 week). The experiments were performed in liquid. The Young's modulus showed an initial sharp increase after an incubation time of 30 min, from a few MPa (native) to 100 MPa. From then onwards we measured a monotonic increase until a saturation value of about 2 GPa was reached after one week. We did not observe a dependence on the elastic modulus evolution using ribose versus glutaraldehyde. The saturation value was very similar to that measured on dry collagen nanoribbons.
Source: europepmc · Quality: candidate unverified · Source record ↗

Research context

OpenAlex topics: Force Microscopy Techniques and Applications · Cellular Mechanics and Interactions · Cell Adhesion Molecules Research

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

Affiliations

Instituto de Ciencia de Materiales de Madrid, CSIC, c/ Sor Juana Inés de la Cruz 3, 28049 Madrid, Spain

Funding

Ministerio de Ciencia, Innovación y Universidades · Consejería de Educación, Juventud y Deporte, Comunidad de Madrid

References (51)

Show source-provided references
1. P.Fratzl , Collagen: Structure and Mechanics, an Introduction , Springer US , 2008 , pp. 1–1310.1007/978-0-387-73906-9 ↗
2. Holmes · Curr. Top. Dev. Biol. · 2018 · 130 · 10710.1016/bs.ctdb.2018.02.004 ↗
3. Kirkness · Curr. Opin. Chem. Biol. · 2019 · 53 · 9810.1016/j.cbpa.2019.08.001 ↗
4. Bielajew · Nat. Rev. Mater. · 2020 · 5 · 73010.1038/s41578-020-0213-1 ↗
5. Kwon · Nanomanuf. Metrol. · 2023 · 6 · 3010.1007/s41871-023-00208-3 ↗
6. Kwon · Commun. Biol. · 2022 · 5 · 122910.1038/s42003-022-04204-z ↗
7. Andriotis · J. R. Soc., Interface · 2015 · 12 · 2015070110.1098/rsif.2015.0701 ↗
8. Baldwin · J. Mech. Behav. Biomed. Mater. · 2016 · 60 · 35610.1016/j.jmbbm.2016.02.004 ↗
9. Stylianou · Scanning · 2019 · 2019 · 845285110.1155/2019/8452851 ↗
10. Gisbert · ACS Nano · 2021 · 15 · 185010.1021/acsnano.0c10159 ↗
11. Panwar · J. Biol. Chem. · 2015 · 290 · 2329110.1074/jbc.M115.644310 ↗
12. Yang · Biophys. J. · 2008 · 94 · 220410.1529/biophysj.107.111013 ↗
13. Buehler · J. Mech. Behav. Biomed. Mater. · 2008 · 1 · 5910.1016/j.jmbbm.2007.04.001 ↗
14. Adamiak · Int. J. Biol. Macromol. · 2020 · 161 · 55010.1016/j.ijbiomac.2020.06.075 ↗
15. Gaar · Org. Chem. Front. · 2020 · 7 · 278910.1039/D0QO00624F ↗
16. Rufin · Acta Biomater. · 2024 · 189 · 20810.1016/j.actbio.2024.08.039 ↗
17. Yang · J. Mech. Behav. Biomed. Mater. · 2012 · 6 · 14810.1016/j.jmbbm.2011.11.008 ↗
18. Haluszka · J. Dent. Res. · 2022 · 101 · 151010.1177/00220345221100404 ↗
19. Sloseris · Matrix Biol. · 2025 · 135 · 15310.1016/j.matbio.2024.12.007 ↗
20. Minary-Jolandan · Biomacromolecules · 2009 · 10 · 256510.1021/bm900519v ↗
21. Vaez · Acta Biomater. · 2023 · 155 · 18210.1016/j.actbio.2022.11.033 ↗
22. Herruzo · Nat. Commun. · 2014 · 5 · 312610.1038/ncomms4126 ↗
23. Kocun · ACS Nano · 2017 · 11 · 1009710.1021/acsnano.7b04530 ↗
24. Benaglia · Nat. Protoc. · 2018 · 13 · 289010.1038/s41596-018-0070-1 ↗
25. Benaglia · Nanoscale · 2019 · 11 · 1528910.1039/C9NR04396A ↗
26. Garcia · Chem. Soc. Rev. · 2020 · 49 · 585010.1039/D0CS00318B ↗
27. Giubertoni · Proc. Natl. Acad. Sci. U. S. A. · 2024 · 121 · e231316212110.1073/pnas.2313162121 ↗
28. Amo · ACS Nano · 2017 · 11 · 865010.1021/acsnano.7b04381 ↗
29. Baldwin · Biophys. J. · 2014 · 107 · 179410.1016/j.bpj.2014.09.003 ↗
30. Vassaux · Biomacromolecules · 2024 · 25 · 480910.1021/acs.biomac.4c00183 ↗
31. Uhlig · Nanoscale · 2017 · 9 · 124410.1039/C6NR07697A ↗
32. Grant · Appl. Phys. Lett. · 2008 · 92 · 23310910.1063/1.2937001 ↗
33. Grant · Biophys. J. · 2009 · 97 · 298510.1016/j.bpj.2009.09.010 ↗
34. Arvelo · J. Chem. Phys. · 2024 · 160 · 16470110.1063/5.0205611 ↗
35. Labuda · Beilstein J. Nanotechnol. · 2016 · 7 · 97010.3762/bjnano.7.89 ↗
36. Garcia · Biophys. J. · 2018 · 114 · 292310.1016/j.bpj.2018.05.012 ↗
37. Gisbert · ACS Nano · 2021 · 15 · 2057410.1021/acsnano.1c09178 ↗
38. Gisbert · Soft Matter · 2023 · 19 · 585710.1039/D3SM00334E ↗
39. Bansode · Sci. Rep. · 2020 · 10 · 339710.1038/s41598-020-60250-9 ↗
40. Mull · Nanoscale Adv. · 2022 · 4 · 482910.1039/D2NA00514J ↗
41. Mesquida · Sci. Rep. · 2018 · 8 · 1012610.1038/s41598-018-28293-1 ↗
42. Garcia-Sacristan · ACS Nano · 2024 · 18 · 1848510.1021/acsnano.4c03839 ↗
43. Leow · Langmuir · 2011 · 27 · 1090710.1021/la2018055 ↗
44. Narayanan · Langmuir · 2014 · 30 · 134310.1021/la4043364 ↗
45. Bellmunt · Lung · 1995 · 173 · 17710.1007/BF00175658 ↗
46. Sell · J. Biol. Chem. · 1989 · 264 · 2159710.1016/S0021-9258(20)88225-8 ↗
47. Ortwerth · Photochem. Photobiol. · 1997 · 65 · 66610.1111/j.1751-1097.1997.tb01909.x ↗
48. Zhang · Food Hydrocolloids · 2022 · 124 · 10727010.1016/j.foodhyd.2021.107270 ↗
49. Yu · Collagen Leather · 2024 · 6 · 2910.1186/s42825-024-00172-8 ↗
50. Labuda · Rev. Sci. Instrum. · 2016 · 87 · 07370510.1063/1.4955122 ↗
51. Garcia-Sacristan · Zenodo · 202510.5281/zenodo.15574388 ↗