Literature DB >> 19627816

Deformation rate controls elasticity and unfolding pathway of single tropocollagen molecules.

Alfonso Gautieri1, Markus J Buehler, Alberto Redaelli.   

Abstract

Collagen is an important structural protein in vertebrates and is responsible for the integrity of many tissues like bone, teeth, cartilage and tendon. The mechanical properties of these tissues are primarily determined by their hierarchical arrangement and the role of the collagen matrix in their structures. Here we report a series of Steered Molecular Dynamics (SMD) simulations in explicit solvent, used to elucidate the influence of the pulling rate on the Young's modulus of individual tropocollagen molecules. We stretch a collagen peptide model sequence [(Gly-Pro-Hyp)(10)](3) with pulling rates ranging from 0.01 to 100 m/s, reaching much smaller deformation rates than reported in earlier SMD studies. Our results clearly demonstrate a strong influence of the loading velocity on the observed mechanical properties. Most notably, we find that Young's modulus converges to a constant value of approximately 4 GPa tangent modulus at 8% tensile strain when the initially crimped molecule is straightened out, for pulling rates below 0.5 m/s. This enables us for the first time to predict the elastic properties of a single tropocollagen molecule at physiologically and experimentally relevant pulling rates, directly from atomistic-level calculations. At deformation rates larger than 0.5 m/s, Young's modulus increases continuously and approaches values in excess of 15 GPa for deformation rates larger than 100 m/s. The analyses of the molecular deformation mechanisms show that the tropocollagen molecule unfolds in distinctly different ways, depending on the loading rate, which explains the observation of different values of Young's modulus at different loading rates. For low pulling rates, the triple helix first uncoils completely at 10%-20% strain, then undergoes some recoiling in the opposite direction, and finally straightens for strains larger than 30%. At intermediate rates, the molecule uncoils linearly with increasing strain up to 35% strain. Finally, at higher velocities the triple helix does not uncoil during stretching.

Entities:  

Mesh:

Substances:

Year:  2008        PMID: 19627816     DOI: 10.1016/j.jmbbm.2008.03.001

Source DB:  PubMed          Journal:  J Mech Behav Biomed Mater        ISSN: 1878-0180


  37 in total

1.  Molecular mechanism of force induced stabilization of collagen against enzymatic breakdown.

Authors:  Shu-Wei Chang; Brendan P Flynn; Jeffrey W Ruberti; Markus J Buehler
Journal:  Biomaterials       Date:  2012-03-06       Impact factor: 12.479

2.  Designed to fail: a novel mode of collagen fibril disruption and its relevance to tissue toughness.

Authors:  Samuel P Veres; J Michael Lee
Journal:  Biophys J       Date:  2012-06-19       Impact factor: 4.033

3.  Atomistic modeling of collagen proteins in their fibrillar environment.

Authors:  Ian Streeter; Nora H de Leeuw
Journal:  J Phys Chem B       Date:  2010-10-21       Impact factor: 2.991

Review 4.  Deformation and failure of protein materials in physiologically extreme conditions and disease.

Authors:  Markus J Buehler; Yu Ching Yung
Journal:  Nat Mater       Date:  2009-03       Impact factor: 43.841

5.  Adaptation of fibrous biopolymers to recurring increasing strains.

Authors:  John W Weisel; Rustem I Litvinov
Journal:  Proc Natl Acad Sci U S A       Date:  2013-07-10       Impact factor: 11.205

6.  Nanomechanics of collagen microfibrils.

Authors:  Simone Vesentini; Alberto Redaelli; Alfonso Gautieri
Journal:  Muscles Ligaments Tendons J       Date:  2013-05-21

7.  Viscoelastic properties of isolated collagen fibrils.

Authors:  Zhilei Liu Shen; Harold Kahn; Roberto Ballarini; Steven J Eppell
Journal:  Biophys J       Date:  2011-06-22       Impact factor: 4.033

8.  Molecular dynamics study on the tensile deformation of cross-linking epoxy resin.

Authors:  Dong R Xin; Qiang Han
Journal:  J Mol Model       Date:  2015-01-22       Impact factor: 1.810

9.  Single molecule effects of osteogenesis imperfecta mutations in tropocollagen protein domains.

Authors:  Alfonso Gautieri; Simone Vesentini; Alberto Redaelli; Markus J Buehler
Journal:  Protein Sci       Date:  2009-01       Impact factor: 6.725

10.  Collagen peptide simulated bending after applied axial deformation.

Authors:  Jonathan W Bourne; Lei Shi; Peter A Torzilli
Journal:  J Mech Behav Biomed Mater       Date:  2020-05-01
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.