Sharp K, Fine R, Honig B
Science. 1987 Jun 12;236(4807):1460-3. doi: 10.1126/science.3589666.
Computer simulations of the diffusion of a substrate to an enzyme active site were performed. They included the detailed shape of the protein and an accurate description of its electrostatic potential. Application of the method to the diffusion of the superoxide anion to the protein superoxide dismutase revealed that the electric field of the enzyme enhances the association rate of the anion by a factor of 30 or more. Calculated changes in the association rate as a function of ionic strength and amino acid modification paralleled the observed behavior. Design principles of superoxide dismutase are considered with respect to insights provided by the simulations. A possible means of enhancing the enzyme turnover rate through site-directed mutagenesis is proposed.
对底物扩散至酶活性位点进行了计算机模拟。这些模拟包括蛋白质的详细形状及其静电势的精确描述。将该方法应用于超氧阴离子向蛋白质超氧化物歧化酶的扩散,结果表明酶的电场使阴离子的缔合速率提高了30倍或更多。计算得出的缔合速率随离子强度和氨基酸修饰的变化与观察到的行为相平行。根据模拟提供的见解,考虑了超氧化物歧化酶的设计原则。提出了一种通过定点诱变提高酶周转速率的可能方法。