# Coarse-grained Martini 3 model for collagen fibrils

## TL;DR

Researchers developed a new computational model for collagen fibrils that includes cross-links, enabling more efficient and accurate simulations of collagen's mechanical properties.

## Contribution

A new coarse-grained Martini 3 model for collagen fibrils with cross-links is introduced, bridging the gap between atomistic and coarse-grained simulations.

## Key findings

- The model was validated against experimental data and all-atom simulations.
- It captures the structural and mechanical behavior of collagen including cross-links.
- The model can be used to study age-related changes in tissue mechanics.

## Abstract

Collagen is a prevalent protein in the Animalia kingdom, especially in mammals. It is abundant in all connective tissue such as bone or ligaments, and thus, it is subjected to substantial mechanical forces. Cross-links play an essential role for the structural and mechanical integrity of collagen, determining its stiffness and rigidity. Until now, studies on collagen including cross-links have either been confined to fully atomistic simulations, which are computationally intensive and restrict the accessible time and length scales, or to coarse-grained descriptions that do not resolve the force response on a residue level and therefore do not consider the triple helical structure and the connectivity of cross-links. To bridge this gap, we report on the development and validation of a computational model based on the Martini 3 coarse-grained force field, in which we parametrized the fibrillar collagen structure including cross-links. We validated the model, through extensive equilibrium and nonequilibrium molecular dynamics simulations, against experimental properties and all-atom simulations. Because the type and distribution of cross-links vary with aging, we expect that this collagen model can be employed to provide insights into age-related changes in tissue mechanics and guide the development of biomimetic materials.