Department of Basic Science, Charles E. Schmidt College of Medicine, Florida Atlantic University, Boca Raton, Florida 33431, USA.
J Biol Chem. 2011 May 13;286(19):16891-9. doi: 10.1074/jbc.M111.222307. Epub 2011 Mar 28.
The avid binding of tissue inhibitors of metalloproteinases (TIMPs) to matrix metalloproteinases (MMPs) is crucial for the regulation of pericellular and extracellular proteolysis. The interactions of the catalytic domain (cd) of MMP-1 with the inhibitory domains of TIMP-1 and TIMP-2 (N-TIMPs) and MMP-3cd with N-TIMP-2 have been characterized by isothermal titration calorimetry and compared with published data for the N-TIMP-1/MMP-3cd interaction. All interactions are largely driven by increases in entropy but there are significant differences in the profiles for the interactions of both N-TIMPs with MMP-1cd as compared with MMP-3cd; the enthalpy change ranges from small for MMP-1cd to highly unfavorable for MMP-3cd (-0.1 ± 0.7 versus 6.0 ± 0.5 kcal mol(-1)). The heat capacity change (ΔC(p)) of binding to MMP-1cd (temperature dependence of ΔH) is large and negative (-210 ± 20 cal K(-1) mol(-1)), indicating a large hydrophobic contribution, whereas the ΔC(p) values for the binding to MMP-3cd are much smaller (-53 ± 3 cal K(-1) mol(-1)), and some of the entropy increase may arise from increased conformational entropy. Apart from differences in ionization effects, it appears that the properties of the MMP may have a predominant influence in the thermodynamic profiles for these N-TIMP/MMP interactions.
细胞外基质金属蛋白酶抑制剂(TIMP)与基质金属蛋白酶(MMP)的强烈结合对于细胞周和细胞外蛋白水解的调控至关重要。MMP-1 的催化结构域(cd)与 TIMP-1 和 TIMP-2(N-TIMP)的抑制结构域以及 MMP-3cd 与 N-TIMP-2 的相互作用已通过等温滴定量热法进行了表征,并与 N-TIMP-1/MMP-3cd 相互作用的已发表数据进行了比较。所有相互作用主要由熵的增加驱动,但 N-TIMP 与 MMP-1cd 相互作用的特征与 MMP-3cd 相比存在显著差异;焓变范围从 MMP-1cd 的较小到 MMP-3cd 的非常不利(-0.1 ± 0.7 与 6.0 ± 0.5 kcal mol(-1))。与 MMP-1cd 结合的热容量变化(ΔC(p))(ΔH 的温度依赖性)较大且为负(-210 ± 20 cal K(-1) mol(-1)),表明存在较大的疏水性贡献,而与 MMP-3cd 结合的 ΔC(p) 值要小得多(-53 ± 3 cal K(-1) mol(-1)),并且部分熵增加可能来自构象熵的增加。除了电离效应的差异外,似乎 MMP 的性质对这些 N-TIMP/MMP 相互作用的热力学特征具有主要影响。