Chen J, Selvin P R
Physics Department and Center for Biophysics, University of Illinois, Urbana, Illinois 61801, USA.
Bioconjug Chem. 1999 Mar-Apr;10(2):311-5. doi: 10.1021/bc980113w.
Thiol-reactive lanthanide complexes have been synthesized that are luminescent when bound to terbium and/or europium. The complexes consist of a diethylenetriaminepentaacetate (DTPA) chelate covalently joined through one amide bond to a chromophore, carbostyril 124, and via a second amide bond to a maleimide, bromoacetamide, or pyridyldithio moiety. Site-specific attachment and characterization of the complexes attached to DNA-activating protein NtrC, to various sites on myosin, or to DNA are presented. The compounds coordinate a surprisingly large number of ligation sites of terbium when a hydrazide spacer is used between the chelate and thiol-reactive moiety, although this extra ligation can cause quenching when europium is used. Synthesis is a simple two- or three-step reaction, and purification is straightforward. The compounds should be useful as nonisotopic replacements, as long-lifetime probes in imaging, and as donors in luminescence resonance energy transfer. They are examples of a wide class of chelates that can be made conjugatable via readily available hetero- or homo-bifunctional linkers.
已经合成了硫醇反应性镧系元素配合物,它们在与铽和/或铕结合时会发光。这些配合物由二乙三胺五乙酸(DTPA)螯合物组成,该螯合物通过一个酰胺键与发色团咔唑124共价连接,并通过第二个酰胺键与马来酰亚胺、溴乙酰胺或吡啶二硫部分连接。本文介绍了这些配合物与DNA激活蛋白NtrC、肌球蛋白上的各个位点或DNA的位点特异性连接及表征。当在螯合物和硫醇反应性部分之间使用酰肼间隔基时,这些化合物能配位数量惊人的铽连接位点,不过当使用铕时,这种额外的配位会导致淬灭。合成是简单的两步或三步反应,纯化也很直接。这些化合物可用作非同位素替代物、成像中的长寿命探针以及发光共振能量转移中的供体。它们是一大类螯合物的实例,这类螯合物可通过容易获得的杂双功能或同双功能连接子实现共轭。