| Literature DB >> 34265261 |
Agnieszka Obarska-Kosinska1, Benedikt Rennekamp2, Aysecan Ünal3, Frauke Gräter4.
Abstract
Type I collagen is the main structural component of many tissues in the human body. It provides excellent mechanical properties to connective tissue and acts as a protein interaction hub. There is thus a wide interest in understanding the properties and diverse functions of type I collagen at the molecular level. A precondition is an atomistic collagen I structure as it occurs in native tissue. To this end, we built full-atom models of cross-linked collagen fibrils by integrating the low-resolution structure of collagen fibril available from x-ray fiber diffraction with high-resolution structures of short collagen-like peptides from x-ray crystallography and mass spectrometry data. We created a Web resource of collagen models for 20 different species with a large variety of cross-link types and localization within the fibril to facilitate structure-based analyses and simulations of type I collagen in health and disease. To easily enable simulations, we provide parameters of the modeled cross-links for an Amber force field. The repository of collagen models is available at https://colbuilder.h-its.org.Entities:
Mesh:
Substances:
Year: 2021 PMID: 34265261 PMCID: PMC8456305 DOI: 10.1016/j.bpj.2021.07.009
Source DB: PubMed Journal: Biophys J ISSN: 0006-3495 Impact factor: 3.699