Krieg R, Halbhuber K J
Institute of Anatomy II, Friedrich Schiller University Jena, Teichgraben 7, D-07743 Jena, Germany.
Cell Mol Biol (Noisy-le-grand). 2003 Jun;49(4):547-63.
Immunoassays have developed to become an important analytical tool in life sciences for detection of endogenous and exogenous targets. Among the most important enzyme labels horseradish peroxidase (HRP), alkaline phosphatase (AP), and beta-D-galactosidase (GAL) is HRP the smallest enzyme and plays nowadays an outstanding role. The oldest substrates are chromogens widely applied for localization of sites of peroxidase (PO) activity in histochemistry as well as for colorimetric applications. They are represented by a diversity of aromatic amines and phenols. Encouraged by development of light excitation and measuring techniques and the commercial availability of highly sensitive equipment, luminescent labels represent the most sensitive and worthwhile detection tools to date. In contrast to chromogens fluorescent labels for detection PO activity are confined only to a few substrates developed more recently. These substrates are mostly applied in histochemistry at a short time scale due to their frequently high solubility. At the long time scale sole exception is so far the tyramine based fluorochome deposition technique (more general: catalytic reporter deposition, CARD). Despite quite different staining behavior both fluorometric and product deposition related principles are based on 4-hydroxy phenylalkyl substrates. The following article reviews basic principles of peroxidatic substrate degradation processes including chromogenic and fluorescent approaches with emphasis on recent advances in development of chromogens and fluorogens for application in histology. As a result of systematic efforts towards the design of substrates, the range of classical precipitating chromogens as well as fluorescent techniques could be complimented by novel highly sensitive substrates with superior staining capabilities: a) Metal chelating 2-hydroxy benzylamines are derived from classical aniline substrates (two steps) and utilize metal catalytic effects in an efficient intramolecular way. The enzymatically yielded dark colored polycondensation products are applicable in histochemistry, in colorimetry and especially as precipitating electron opaque labels with enhanced osmiophilic properties for light and electron microscopy. b) Fluorescent 4-hydroxy-styryl derivatives are capable of oxidative selfanchoring reactions at the cellular level close to sites of PO activity. In contrast to deposition of tyramine conjugated fluorochromes an altered fluorochrome with improved fluorescence properties is furnished during oxidative crosslinking of the substrate. This results in a highly specific and photostable fluorescence response and an outstanding low background staining. Histochemical and immunohistochemical applications are presented.
免疫测定已发展成为生命科学中用于检测内源性和外源性靶标的重要分析工具。在最重要的酶标记物辣根过氧化物酶(HRP)、碱性磷酸酶(AP)和β-D-半乳糖苷酶(GAL)中,HRP是最小的酶,目前发挥着突出的作用。最古老的底物是色原,广泛应用于组织化学中过氧化物酶(PO)活性位点的定位以及比色法应用。它们由多种芳香胺和酚类代表。受光激发和测量技术发展以及高灵敏度设备商业可用性的鼓舞,发光标记物是迄今为止最灵敏且值得使用的检测工具。与色原不同,用于检测PO活性的荧光标记物仅局限于最近开发的少数几种底物。由于这些底物通常具有高溶解性,它们大多在短时间尺度上应用于组织化学。从长时间尺度来看,到目前为止唯一的例外是基于酪胺的荧光染料沉积技术(更一般地说:催化报告沉积,CARD)。尽管荧光测定和产物沉积相关原理的染色行为有很大不同,但两者都基于4-羟基苯基烷基底物。以下文章综述了过氧化物酶底物降解过程的基本原理,包括发色和荧光方法,重点介绍了用于组织学的色原和荧光原开发的最新进展。通过对底物设计的系统性努力,经典的沉淀色原以及荧光技术的范围可以通过具有卓越染色能力的新型高灵敏度底物得到补充:a)金属螯合2-羟基苄胺是由经典苯胺底物衍生而来(两步法),并以高效的分子内方式利用金属催化作用。酶促产生的深色缩聚产物可应用于组织化学、比色法,特别是作为具有增强嗜锇性的沉淀电子不透明标记物用于光学和电子显微镜。b)荧光4-羟基苯乙烯基衍生物能够在细胞水平上靠近PO活性位点发生氧化自锚定反应。与酪胺共轭荧光染料的沉积不同,在底物的氧化交联过程中会产生一种具有改善荧光特性的改变的荧光染料。这导致了高度特异性和光稳定的荧光响应以及出色的低背景染色。还介绍了组织化学和免疫组织化学应用。