Liu H Y, Peltz G A, Leytus S P, Livingston C, Brocklehurst J, Mangel W F
Proc Natl Acad Sci U S A. 1980 Jul;77(7):3796-800. doi: 10.1073/pnas.77.7.3796.
A sensitive in situ assay for the plasminogen activator of transformed cells is described; it uses the fluorogenic molecule 3',6'-bis(4-guanidinobenzoyloxy)-5-(N'-4-carboxylphenyl)thioureidospiro[isobenz ofuran-1(3H),9'-[9H]xanthen]-3-one. This fluorescein derivative is an excellent active-site titrant of the esterase activity of plasmin. When transformed cells are incubated with purified plasminogen and the resulting plasmin is titrated with the fluorogenic substrate, the amount of plasmin formed is linearly proportional to time and cell number. The assay is sensitive enough to detect quantitatively the plasminogen activator activity of as few as 250 transformed cells. This substrate should be useful in studying quantitatively the correlation between increased levels of plasminogen activator activity and cellular transformation and as a general active site titrant of serine proteases.
本文描述了一种用于检测转化细胞纤溶酶原激活剂的灵敏原位测定法;它使用荧光分子3',6'-双(4-胍基苯甲酰氧基)-5-(N'-4-羧基苯基)硫脲基螺[异苯并呋喃-1(3H),9'-[9H]呫吨]-3-酮。这种荧光素衍生物是纤溶酶酯酶活性的优良活性位点滴定剂。当将转化细胞与纯化的纤溶酶原一起孵育,并用荧光底物滴定产生的纤溶酶时,形成的纤溶酶量与时间和细胞数量呈线性比例。该测定法灵敏度足够高,能够定量检测低至250个转化细胞的纤溶酶原激活剂活性。这种底物在定量研究纤溶酶原激活剂活性水平升高与细胞转化之间的相关性以及作为丝氨酸蛋白酶的通用活性位点滴定剂方面应该是有用的。