Barth A, Kreutz W, Mäntele W
Institut für Biophysik und Strahlenbiologie, Universität Frèiburg, Germany.
FEBS Lett. 1990 Dec 17;277(1-2):147-50. doi: 10.1016/0014-5793(90)80830-c.
Fourier transform infrared spectroscopy was used to study ligand binding and conformational changes in the Ca2(+)-ATPase of sarcoplasmic reticulum. Novel in infrared difference spectroscopy, the catalytic cycle in the IR sample was started by photolytic release of ATP from an inactive, photolabile ATP-derivative (caged ATP). Small, but characteristic infrared absorbance changes were observed upon ATP release. On the basis of model spectra, the absorbance changes corresponding to the trigger and substrate reactions, i.e. to photolysis of caged ATP and hydrolysis of ATP, were separated from the absorbance changes due to the active ATPase reflecting formation of the phosphorylated Ca2E1P enzyme form. A major rearrangement of ATPase conformation as the result of catalysis can be excluded.
傅里叶变换红外光谱法被用于研究肌浆网Ca2(+)-ATP酶中的配体结合和构象变化。在红外差示光谱法中,红外样品中的催化循环通过从一种无活性的、光不稳定的ATP衍生物(笼形ATP)光解释放ATP来启动。ATP释放时观察到了微小但具有特征性的红外吸光度变化。根据模型光谱,将对应于触发反应和底物反应(即笼形ATP的光解和ATP的水解)的吸光度变化与反映磷酸化Ca2E1P酶形式形成的活性ATP酶引起的吸光度变化区分开来。可以排除催化作用导致ATP酶构象发生重大重排的可能性。