Takada A, Takada Y
Thromb Res. 1985 Oct 15;40(2):189-97. doi: 10.1016/0049-3848(85)90329-9.
Glu-plasminogen (plg) or Lys-plg solution was kept at pH 2.0 for various time intervals, and then readjusted to pH 7.0. The activation rate and conformational changes of such acid-treated plg were measured using the hydrolysis of S-2251, spectrofluorometry and spectropolarimetry (circular dichroism). The activation rate of acid-treated Glu-plg increased after readjustment to pH 7.0. The increase was not reversible even after keeping acid-treated Glu-plg for 24 hrs at neutral pH. The activation rate of acid-treated Lys-plg rather decreased. The fluorescence intensity at 340 nm of acid-treated plg decreased, and the intensity of fluorescence induced by the interaction of plasminogen with ANS (1-anilino-8-naphthalene sulfonate) increased after keeping plasminogen for longer than 24 hrs at pH 2.0. Circular dichroism spectra indicated that the secondary and tertiary structure of Glu-plg changed after acidification, and that only the tertiary structure of Lys-plg changed.
将谷氨酸纤溶酶原(plg)或赖氨酸纤溶酶原(Lys-plg)溶液在pH 2.0下保持不同的时间间隔,然后重新调节至pH 7.0。使用S-2251水解、荧光光谱法和旋光光谱法(圆二色性)测量这种经酸处理的纤溶酶原的活化率和构象变化。重新调节至pH 7.0后,经酸处理的谷氨酸纤溶酶原的活化率增加。即使在中性pH下将经酸处理的谷氨酸纤溶酶原保持24小时后,这种增加也不可逆。经酸处理的赖氨酸纤溶酶原的活化率反而降低。在pH 2.0下将纤溶酶原保持超过24小时后,经酸处理的纤溶酶原在340 nm处的荧光强度降低,并且纤溶酶原与ANS(1-苯胺基-8-萘磺酸盐)相互作用诱导的荧光强度增加。圆二色性光谱表明,酸化后谷氨酸纤溶酶原的二级和三级结构发生了变化,而赖氨酸纤溶酶原仅三级结构发生了变化。