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Mechanical Load Induces a 100-Fold Increase in the Rate of Collagen Proteolysis by MMP-1

机译:机械负荷导致MMP-1胶原蛋白水解速率增加100倍

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摘要

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.
机译:尽管已知机械应力会深刻影响细胞外基质(ECM)的组成和结构,但对该调节发生的机理仍知之甚少。我们使用单分子镊子测定法来研究力对基质金属蛋白酶-1(MMP-1)对胶原蛋白水解的影响。在这里,我们表明在拉伸力中施加约10 pN会导致蛋白水解率增加约100倍。我们的结果支持了一种机械模型,其中胶原蛋白三螺旋在蛋白水解之前解开。数据和所得模型预测,生物学相关力可能会增加局部ECM蛋白水解作用,表明机械力在ECM重塑调节中可能发挥作用。

著录项

  • 来源
    《Journal of the American Chemical Society》 |2011年第6期|p.1686-1689|共4页
  • 作者单位

    Department of Chemical Engineering, Stanford University, Stanford, California 94305, United States;

    Department of Chemical Engineering, Stanford University, Stanford, California 94305, United States;

    Department of Chemical Engineering, Stanford University, Stanford, California 94305, United States;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
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  • 入库时间 2022-08-18 03:14:05

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