Cox S W, Cho K, Eley B M, Smith R E
Department of Periodontology, King's College School of Medicine and Dentistry, London, U.K.
J Periodontal Res. 1990 May;25(3):164-71. doi: 10.1111/j.1600-0765.1990.tb01039.x.
Substrate impregnated paper discs were prepared using peptidyl derivatives of 7-amino-4-trifluoromethylcoumarin (AFC). After incubation with test solutions, the green, UV-induced fluorescence of AFC liberated by enzyme activity was distinguishable from the blue-violet fluorescence of the substrates. The AFC could then be coupled with p-dimethylaminocinnamaldehyde to form a colored Schiff base. Semi-quantiative assessments of disc fluorescence and color were made by comparison with AFC/substrate standards. Assays with discs impregnated with MeOSuc-Ala-Ala-Pro-Val-AFC, Z-Gly-Gly-Arg-AFC and Ala-Pro-AFC for elastase-, trypsin-, and dipeptidyl peptidase (DPP) IV-like activities respectively were evaluated using purified DPP IV and 100 eluates of crevicular fluid collected on filter paper strips from 10 gingivitis and periodontitis patients. The results showed that, within their working ranges, scores of disc fluorescence and color were reasonably accurate and reliable by comparison with enzyme activities measured in parallel quantitative fluorimetric assays with the same substrates. Using disc color, which was more sensitive than fluorescence, it was generally possible to measure all three enzyme activities in crevicular fluid samples from 5 periodontitis patients with varying degrees of gingival inflammation and pocketing. Disc color assays require no special apparatus and could be used for enzyme estimations in the clinical setting.
使用7-氨基-4-三氟甲基香豆素(AFC)的肽基衍生物制备底物浸渍纸片。与测试溶液孵育后,酶活性释放的AFC产生的绿色紫外线诱导荧光与底物的蓝紫色荧光可区分开来。然后,AFC可与对二甲氨基肉桂醛偶联形成有色席夫碱。通过与AFC/底物标准品比较,对纸片荧光和颜色进行半定量评估。分别用浸渍有MeOSuc-Ala-Ala-Pro-Val-AFC、Z-Gly-Gly-Arg-AFC和Ala-Pro-AFC的纸片检测弹性蛋白酶、胰蛋白酶和二肽基肽酶(DPP)IV样活性,使用纯化的DPP IV和从10名牙龈炎和牙周炎患者的滤纸带上收集的100份龈沟液洗脱液进行评估。结果表明,在其工作范围内,与使用相同底物的平行定量荧光测定法测得的酶活性相比,纸片荧光和颜色评分相当准确可靠。使用比荧光更敏感的纸片颜色,通常可以测量5名不同程度牙龈炎症和牙周袋深度的牙周炎患者龈沟液样本中的所有三种酶活性。纸片颜色测定法不需要特殊仪器,可用于临床环境中的酶测定。