Computational insights into the substrate recognition mechanism of cartilage extracellular matrix degradation

Yen-Yu Lai; Deng Li; Shu-Wei Chang

doi:10.1016/j.csbj.2021.10.002

Computational insights into the substrate recognition mechanism of cartilage extracellular matrix degradation

Comput Struct Biotechnol J. 2021 Oct 6:19:5535-5545. doi: 10.1016/j.csbj.2021.10.002. eCollection 2021.

Authors

Yen-Yu Lai¹, Deng Li¹, Shu-Wei Chang^{1

2}

Affiliations

¹ National Taiwan University, Department of Civil Engineering, Taipei 10617, Taiwan.
² National Taiwan University, Department of Biomedical Engineering, Taipei 10617, Taiwan.

Abstract

Articular cartilage is connective tissue that forms a slippery load-bearing joint surface between bones. With outstanding mechanical properties, it plays an essential role in cushioning impact and protecting the ends of bones. Abnormal mechanical stimulation, such as repetitive overloading or chondral injury, induces excessive cartilage extracellular matrix (ECM) degradation, leading to osteoarthritis and other joint disorders. A disintegrin and metalloproteinase with thrombospondin motifs-5 (ADAMTS-5) is an aggrecanase that dominates the catalysis of aggrecan, the major proteoglycan in the cartilage ECM. Intriguingly, unlike its critical cleavage site Glu³⁷³-³⁷⁴Ala, another potential cleavage site, Glu⁴¹⁹-⁴²⁰Ala, composed of the same amino acids in the aggrecan interglobular domain, is not a major cleavage site. It remains unclear how ADAMTS-5 distinguishes between them and hydrolyzes the correct scissile bonds. This research introduces a bottom-up in silico approach to reveal the molecular mechanism by which ADAMTS-5 recognizes the cleavage site on aggrecan. It is hypothesized that the sequence in the vicinity assists ADAMTS-5 in positioning the cleavage site. Specific residues were found to serve as binding sites, helping aggrecan bind more stably and fit into the enzyme better. The findings provide insight into the substrate binding and recognition mechanism for cartilage ECM degradation from a brand new atomic-scale perspective, laying the foundation for prophylaxis and treatment of related joint diseases.

Keywords: ADAMTS-5; Aggrecan; Degradation; Extracellular matrix; Molecular dynamics; Osteoarthritis.