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Mechanical Load Induces a 100-Fold Increase in the Rate of Collagen Proteolysis by MMP-1
- Source :
- Journal of the American Chemical Society. 133:1686-1689
- Publication Year :
- 2011
- Publisher :
- American Chemical Society (ACS), 2011.
-
Abstract
- Although mechanical stress is known to profoundly influence the composition and structure of the extracellular matrix (ECM), the mechanisms by which this regulation occurs remain poorly understood. We used a single-molecule magnetic tweezers assay to study the effect of force on collagen proteolysis by matrix metalloproteinase-1 (MMP-1). Here we show that the application of ∼10 pN in extensional force causes an ∼100-fold increase in proteolysis rates. Our results support a mechanistic model in which the collagen triple helix unwinds prior to proteolysis. The data and resulting model predict that biologically relevant forces may increase localized ECM proteolysis, suggesting a possible role for mechanical force in the regulation of ECM remodeling.
- Subjects :
- Models, Molecular
Magnetic tweezers
Mechanical Phenomena
Collagen helix
Proteolysis
Kinetics
Molecular Sequence Data
Biophysics
Matrix metalloproteinase
Biochemistry
Article
Catalysis
Extracellular matrix
Colloid and Surface Chemistry
medicine
Amino Acid Sequence
Protein Structure, Quaternary
Mechanical load
medicine.diagnostic_test
Chemistry
General Chemistry
Peptide Fragments
Collagen
Matrix Metalloproteinase 1
Protein Multimerization
Subjects
Details
- ISSN :
- 15205126 and 00027863
- Volume :
- 133
- Database :
- OpenAIRE
- Journal :
- Journal of the American Chemical Society
- Accession number :
- edsair.doi.dedup.....70ec194ba53140f2eef767c2b9c6f5a1