2016 journal article

Tensile mechanical properties of collagen type I and its enzymatic crosslinks

BIOPHYSICAL CHEMISTRY, 214, 1–10.

co-author countries: United States of America πŸ‡ΊπŸ‡Έ
author keywords: Type I collagen; Microfibril; Enzyme-derived crosslink; Molecular dynamics
MeSH headings : Amino Acids; Bone and Bones / physiology; Collagen Type I / chemistry; Cross-Linking Reagents; Dipeptides; Elastic Modulus; Enzymes; Humans; Microfibrils / chemistry; Models, Molecular; Molecular Dynamics Simulation; Skin Physiological Phenomena; Structure-Activity Relationship; Tensile Strength
Source: Web Of Science
Added: August 6, 2018

Collagen type I crosslink type and prevalence can be influenced by age, tissue type, and health; however, the role that crosslink chemical structure plays in mechanical behavior is not clear. Molecular dynamics simulations of ~65-nm-long microfibril units were used to predict how difunctional (deH-HLNL and HLKNL) and trifunctional (HHL and PYD) crosslinks respond to mechanical deformation. Low- and high-strain stress-strain regions were observed, corresponding to crosslink alignment. The high-strain elastic moduli were 37.7, 37.9, 39.9, and 42.4 GPa for the HLKNL, deH-HLNL, HHL, and PYD-crosslinked models, respectively. Bond dissociation analysis suggests that PYD is more brittle than HHL, with deH-HLNL and HLKNL being similarly ductile. These results agree with the tissues in which these crosslinks are found (e.g., deH-HLNL/HLKNL in developing tissues, HHL in mature skin, and PYD in mature bone). Chemical structure-function relationships identified for these crosslinks can aid the development of larger-scale models of collagenous tissues and materials.