Chemical Engineering Department, Bogazici University, Bebek, 34342 Istanbul, Turkey.
Comput Biol Chem. 2013 Apr;43:1-10. doi: 10.1016/j.compbiolchem.2012.12.002. Epub 2012 Dec 12.
Bacterial production of beta-lactamases, which hydrolyze beta-lactam type antibiotics, is a common antibiotic resistance mechanism. Antibiotic resistance is a high priority intervention area and one strategy to overcome resistance is to administer antibiotics with beta-lactamase inhibitors in the treatment of infectious diseases. Unfortunately, beta-lactamases are evolving at a rapid pace with new inhibitor resistant mutants emerging every day, driving the design and development of novel beta-lactamase inhibitors. Here, we examined the inhibitor recognition mechanism of two common beta-lactamases using molecular dynamics simulations. Binding of beta-lactamase inhibitor protein (BLIP) caused changes in the flexibility of regions away from the binding site. One of these regions was the H10 helix, which was previously identified to form a lid over an allosteric inhibitor binding site. Closer examination of the H10 helix using sequence and structure comparisons with other beta-lactamases revealed the presence of a highly conserved Trp229 residue, which forms a stacking interaction with two conserved proline residues. Molecular dynamics simulations on the Trp229Ala mutants of TEM-1 and SHV-1 resulted in decreased stability in the apo form, possibly due to loss of the stacking interaction as a result of the mutation. The mutant TEM-1 beta-lactamase had higher H10 fluctuations in the presence of BLIP, higher affinity to BLIP and higher cross-correlations with BLIP. Our results suggest that the H10 helix and specifically W229 are important modulators of the allosteric communication between the active site and the allosteric site.
细菌产生β-内酰胺酶,水解β-内酰胺类抗生素,是一种常见的抗生素耐药机制。抗生素耐药是一个高度优先的干预领域,克服耐药的一种策略是在治疗感染性疾病时使用具有β-内酰胺酶抑制剂的抗生素。不幸的是,β-内酰胺酶正在以惊人的速度进化,每天都有新的抑制剂耐药突变体出现,这促使我们设计和开发新型β-内酰胺酶抑制剂。在这里,我们使用分子动力学模拟研究了两种常见β-内酰胺酶的抑制剂识别机制。β-内酰胺酶抑制剂蛋白(BLIP)的结合导致远离结合位点的区域的灵活性发生变化。其中一个区域是 H10 螺旋,它以前被确定为在变构抑制剂结合位点上方形成一个盖子。通过与其他β-内酰胺酶的序列和结构比较,更仔细地检查 H10 螺旋,发现存在一个高度保守的色氨酸残基 229,它与两个保守的脯氨酸残基形成堆积相互作用。TEM-1 和 SHV-1 的 Trp229Ala 突变体的分子动力学模拟导致apo 形式的稳定性降低,可能是由于突变导致堆积相互作用的丧失。突变的 TEM-1 β-内酰胺酶在存在 BLIP 时具有更高的 H10 波动、更高的 BLIP 亲和力和更高的 BLIP 交叉相关性。我们的结果表明,H10 螺旋,特别是 W229,是活性位点和变构位点之间变构通讯的重要调节剂。