Tung J S, Mark G E, Hollis G F
Department of Cellular and Molecular Biology, Merck Research Laboratories, Rahway, New Jersey 07065.
Anal Biochem. 1994 Nov 15;223(1):149-52. doi: 10.1006/abio.1994.1560.
A sensitive, high-throughput assay has been developed which measures hyaluronidase activity in a microplate format. In this assay, hyaluronic acid is suspended in agarose in a microtiter well, the plate is incubated with the hyaluronidase solution, and the undigested hyaluronic acid is precipitated with cetylpyridinium chloride. The precipitate blocks light transmittance and therefore an increase in the visible light transmitted correlates with the amount of digested hyaluronic acid. Using this assay, as little as 0.05 units of hyaluronidase activity can be detected. The assay is highly reproducible and can be run with commercially available reagents. Hyaluronidase activity is easy to quantitate using a microplate reader and this format allows large numbers of samples to be assayed.
已开发出一种灵敏的高通量检测方法,该方法以微孔板形式测量透明质酸酶活性。在该检测中,透明质酸悬浮于微量滴定孔中的琼脂糖中,将平板与透明质酸酶溶液一起孵育,未消化的透明质酸用十六烷基吡啶氯化物沉淀。沉淀物会阻碍透光率,因此透射可见光的增加与消化的透明质酸量相关。使用该检测方法,可检测低至0.05单位的透明质酸酶活性。该检测具有高度可重复性,并且可以使用市售试剂进行。使用微孔板读数器很容易对透明质酸酶活性进行定量,并且这种形式允许检测大量样品。