Department Chemistry and Biochemistry, University of Notre Dame , Notre Dame, Indiana 46556, United States.
Biochemistry. 2014 Mar 18;53(10):1548-50. doi: 10.1021/bi500074w. Epub 2014 Mar 3.
β-Lactam antibiotics have faced obsolescence with the emergence of methicillin-resistant Staphylococcus aureus (MRSA). A complex set of events ensues upon exposure of MRSA to these antibiotics, which culminates in proteolysis of BlaI or MecI, two gene repressors, and results in the induction of resistance. We report studies on the mechanism of binding of these gene repressors to the operator regions by fluorescence anisotropy. Within the range of in vivo concentrations for BlaI and MecI, these proteins interact with their regulatory elements in a reversible manner, as both a monomer and a dimer.
β-内酰胺类抗生素在耐甲氧西林金黄色葡萄球菌(MRSA)出现后面临淘汰。当 MRSA 暴露于这些抗生素时,会发生一系列复杂的事件,最终导致两个基因抑制剂 BlaI 或 MecI 的蛋白水解,从而导致耐药性的诱导。我们通过荧光各向异性报告了这些基因抑制剂与操纵子区域结合的机制研究。在 BlaI 和 MecI 的体内浓度范围内,这些蛋白质以可逆的方式与它们的调节元件相互作用,无论是单体还是二聚体。