Steven F S, Lowther D A
Connect Tissue Res. 1975;4(1):7-10. doi: 10.3109/03008207509152191.
98% of the collagen in mature connective tissue is in the form of insoluble collagen fibers, consisting of bundles of polymeric collagen (PC) fibrils. The enzymes concerned in connective tissue remodeling degrade PC rather than tropocollagen (TC). TC is the most usual substrate for collagenase assays, and we believe it is essential to employ PC in any study of the activity of collagenolytic enzymes. In order to facilitate the study of enzymic degradation of PC we have labelled PC with fluorescein iso-thiocyanate to produce F-PC fibrils, containing 5 fluorescein labelled epilson-NH2 groups of lysine per TC molecule within the PC. The fluorescent F-PC is degraded at the same rate as PC with the release of hydroxyprolyl peptides but has the great advantage that the solubilised F-peptides can be quantitated by their fluorescent emission. The technique is described in detail employing bacterial collagenase and mammalian collagenase preparations to illustrate the methodology. The advantages of the fluorescent technique over the collagenolytic assay methods currently in use are outlined.
成熟结缔组织中98%的胶原蛋白是以不溶性胶原纤维的形式存在,由聚合胶原(PC)原纤维束组成。参与结缔组织重塑的酶降解的是PC而非原胶原(TC)。TC是胶原酶测定中最常用的底物,我们认为在任何关于胶原olytic酶活性的研究中使用PC都是至关重要的。为了便于研究PC的酶促降解,我们用异硫氰酸荧光素标记PC以产生F-PC原纤维,在PC内每个TC分子含有5个荧光素标记的赖氨酸的ε-NH2基团。荧光F-PC与PC以相同的速率降解并释放羟脯氨酰肽,但具有很大的优势,即溶解的F-肽可以通过其荧光发射进行定量。详细描述了使用细菌胶原酶和哺乳动物胶原酶制剂来说明该方法的技术。概述了荧光技术相对于目前使用的胶原olytic测定方法的优势。