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细胞裂解物和上清液中纤溶酶原激活剂的灵敏荧光测定法。

Sensitive fluorometric determination of plasminogen activator in cell lysates and supernatants.

作者信息

Obrénovitch A, Maintier C, Maillet T, Mayer R, Kieda C, Monsigny M

出版信息

FEBS Lett. 1983 Jul 4;157(2):265-70. doi: 10.1016/0014-5793(83)80559-6.

Abstract

A fluorogenic substrate for plasmin, CBZ-Gly-Pro-Arg-AEC, has been synthesized and used to develop a new sensitive photometric and fluorometric assay of plasminogen activator activity. The fluorescence intensity of free AEC at 460 nm is about 3 orders of magnitude higher than that of acyl-AEC. The release of AEC from the peptidyl derivative was monitored fluorometrically after extraction of free AEC in ethylacetate. Under such conditions, the Km was 0.16 mM. This method was used to monitor the activity of plasminogen activator synthetized by fibroblastic cells (BHK 21 C 13) either released in the supernatants or cell-associated.

摘要

一种用于纤溶酶的荧光底物CBZ-Gly-Pro-Arg-AEC已被合成,并用于开发一种新的灵敏的纤溶酶原激活剂活性的光度法和荧光法测定方法。游离AEC在460nm处的荧光强度比酰基-AEC高约3个数量级。在乙酸乙酯中提取游离AEC后,通过荧光法监测AEC从肽基衍生物中的释放。在这种条件下,米氏常数为0.16mM。该方法用于监测成纤维细胞(BHK 21 C 13)合成的纤溶酶原激活剂的活性,该激活剂可释放到上清液中或与细胞相关。

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