Mokdad Audrey, Nissen Mark, Satterlee James D, Larsen Randy W
Department of Chemistry, University of South Florida, 4202 East Fowler Ave., Tampa, FL 33620, United States.
FEBS Lett. 2007 Sep 18;581(23):4512-8. doi: 10.1016/j.febslet.2007.08.031. Epub 2007 Aug 24.
Here we report the results of transient absorption and photoacoustic calorimetry studies of CO photodissociation from the heme domain of the bacterial oxygen sensor HemAT-Bs. The results indicate that CO photolysis is accompanied by an overall DeltaH of -19 kcal mol(-1) and DeltaV of +4 ml mol(-1) as well as a red-shifted kinetic difference spectrum all occurring in <50 ns. Analysis of the DeltaH/DeltaV reveals that a conformational change takes place with a DeltaH(conf) of -40 kcal mol(-1) and DeltaV(conf) of -22 ml mol(-1). These thermodynamic changes are consistent with an increase in the solvent accessible surface area of the protein upon ligand dissociation, as observed in the X-ray structure of the ferric CN-bound and CN free forms of HemAT-Bs.
在此,我们报告了对细菌氧传感器HemAT-Bs血红素结构域中CO光解离的瞬态吸收和光声量热法研究结果。结果表明,CO光解伴随着-19 kcal mol⁻¹的总ΔH和+4 ml mol⁻¹的ΔV,以及在<50 ns内出现的红移动力学差异光谱。对ΔH/ΔV的分析表明,发生了构象变化,其ΔH(conf)为-40 kcal mol⁻¹,ΔV(conf)为-22 ml mol⁻¹。这些热力学变化与配体解离后蛋白质溶剂可及表面积的增加一致,正如在HemAT-Bs的铁氰根结合和无氰根形式的X射线结构中所观察到的那样。