4.4 Editorial Material

The quest for substrates and binding partners: A critical barrier for understanding the role of ADAMTS proteases in musculoskeletal development and disease

期刊

DEVELOPMENTAL DYNAMICS
卷 250, 期 1, 页码 8-26

出版社

WILEY
DOI: 10.1002/dvdy.248

关键词

ADAMTS-like proteins; connective tissue; degradomics; extracellular matrix; N-terminomics; protease

资金

  1. Ines Mandl Research Foundation
  2. National Institutes of Health [RO1AR070748]
  3. Leni & Peter W. May Department for Orthopaedics

向作者/读者索取更多资源

ADAMTS metalloproteases play a crucial role in musculoskeletal development and disease, with mutations leading to congenital musculoskeletal disorders. The focus should be on understanding the physiological substrates of ADAMTS proteases and the consequences of substrate cleavage, as well as on identifying and validating novel substrates and binding partners to further enhance our knowledge in this area.
Secreted ADAMTS metalloproteases are involved in the sculpting, remodeling, and erosion of connective tissues throughout the body, including in the musculoskeletal system. ADAMTS proteases contribute to musculoskeletal development, pathological tissue destruction, and are mutated in congenital musculoskeletal disorders. Examples include versican cleavage by ADAMTS9 which is required for interdigital web regression during limb development, ADAMTS5-mediated aggrecan degradation in osteoarthritis resulting in joint erosion, and mutations inADAMTS10orADAMTS17that cause Weill-Marchesani syndrome, a short stature syndrome with bone, joint, muscle, cardiac, and eye involvement. Since the function of ADAMTS proteases and proteases in general is primarily defined by the molecular consequences of proteolysis of their respective substrates, it is paramount to identify all physiological substrates for each individual ADAMTS protease. Here, we review the current knowledge of ADAMTS proteases and their involvement in musculoskeletal development and disease, focusing on some of their known physiological substrates and the consequences of substrate cleavage. We further emphasize the critical need for the identification and validation of novel ADAMTS substrates and binding partners by describing the principles of mass spectrometry-based approaches and by emphasizing strategies that need to be considered for validating the physiological relevance for ADAMTS-mediated proteolysis of novel putative substrates.

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