Pujadas G, Palau J
Unitat de Biotecnologia Computacional, Departament de Bioquímica i Biotecnologia, Universitat Rovira i Virgili, Tarragona, Catalonia, Spain.
Protein Sci. 2001 Aug;10(8):1645-57. doi: 10.1110/ps.8201.
Soybean beta-amylase (EC 3.2.1.2) has been crystallized both free and complexed with a variety of ligands. Four water molecules in the free-enzyme catalytic cleft form a multihydrogen-bond network with eight strategic residues involved in enzyme-ligand hydrogen bonds. We show here that the positions of these four water molecules are coincident with the positions of four potential oxygen atoms of the ligands within the complex. Some of these waters are displaced from the active site when the ligands bind to the enzyme. How many are displaced depends on the shape of the ligand. This means that when one of the four positions is not occupied by a ligand oxygen atom, the corresponding water remains. We studied the functional/structural role of these four waters and conclude that their presence means that the conformation of the eight side chains is fixed in all situations (free or complexed enzyme) and preserved from unwanted or forbidden conformational changes that could hamper the catalytic mechanism. The water structure at the active pocket of beta-amylase is therefore essential for providing the ligand recognition process with plasticity. It does not affect the protein active-site geometry and preserves the overall hydrogen-bonding network, irrespective of which ligand is bound to the enzyme. We also investigated whether other enzymes showed a similar role for water. Finally, we discuss the potential use of these results for predicting whether water molecules can mimic ligand atoms in the active center.
大豆β-淀粉酶(EC 3.2.1.2)已被结晶,其形式既有游离态的,也有与多种配体复合的。游离酶催化裂隙中的四个水分子与参与酶-配体氢键形成的八个关键残基形成了多氢键网络。我们在此表明,这四个水分子的位置与复合物中配体的四个潜在氧原子的位置重合。当配体与酶结合时,其中一些水分子会从活性位点被取代。被取代的水分子数量取决于配体的形状。这意味着当四个位置之一未被配体氧原子占据时,相应的水分子会保留下来。我们研究了这四个水分子的功能/结构作用,并得出结论,它们的存在意味着八条侧链的构象在所有情况下(游离或复合酶)都是固定的,并且能避免可能阻碍催化机制的有害或不允许的构象变化。因此,β-淀粉酶活性口袋处的水结构对于为配体识别过程提供可塑性至关重要。它不影响蛋白质活性位点的几何形状,并保留了整体氢键网络,而与结合到酶上的配体无关。我们还研究了其他酶是否对水有类似的作用。最后,我们讨论了这些结果在预测水分子是否能在活性中心模拟配体原子方面的潜在用途。