首页> 美国卫生研究院文献>Scientific Reports >Ultra Q-bodies: quench-based antibody probes that utilize dye-dye interactions with enhanced antigen-dependent fluorescence
【2h】

Ultra Q-bodies: quench-based antibody probes that utilize dye-dye interactions with enhanced antigen-dependent fluorescence

机译:Ultra Q抗体:基于淬灭的抗体探针利用染料与染料的相互作用以及增强的抗原依赖性荧光

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Recently, we described a novel reagentless fluorescent biosensor strategy named Quenchbody, which functions via the antigen-dependent removal of the quenching effect on a fluorophore that is attached to a single-chain antibody variable region. To explore the practical utility of Quenchbodies, we prepared antibody Fab fragments that were fluorolabeled at either one or two of the N-terminal regions, using a cell-free translation-mediated position-specific protein labeling system. Unexpectedly, the Fab fragment labeled at the heavy chain N-terminal region demonstrated a deeper quenching and antigen-dependent release compared to that observed using scFv. Moreover, when the Fab was fluorolabeled at the two N-termini with either the same dye or with two different dyes, an improved response due to enhanced quenching via dye-dye interactions was observed. On the basis of this approach, several targets, including peptides, proteins, and haptens, as well as narcotics, were quantified with a higher response up to 50-fold. In addition, differentiation of osteosarcoma to osteoblasts was successfully imaged using a similarly fluorolabeled recombinant Fab protein prepared from E. coli. Due to its versatility, this “Ultra-Quenchbody” is expected to exhibit a range of applications from in vitro diagnostics to the live imaging of various targets in situ.
机译:最近,我们描述了一种名为Quenchbody的新型无试剂荧光生物传感器策略,该策略通过对依赖于单链抗体可变区的荧光团的抗原依赖性去除作用而起作用。为了探索淬灭抗体的实用性,我们使用无细胞翻译介导的位置特异性蛋白质标记系统,制备了在一个或两个N端区域进行了荧光标记的Fab抗体片段。出乎意料的是,与使用scFv观察到的相比,在重链N端区域标记的Fab片段表现出更深的淬灭和抗原依赖性释放。此外,当用相同的染料或两种不同的染料在两个N末端对Fab进行氟标记时,观察到由于通过染料-染料相互作用的淬灭作用增强而引起的响应改善。在此方法的基础上,定量了包括肽,蛋白质和半抗原以及麻醉药在内的多个目标,其响应高达50倍。另外,使用从大肠杆菌制备的类似的荧光标记的重组Fab蛋白成功地成像了骨肉瘤向成骨细胞的分化。由于其多功能性,这种“超猝灭体”有望展现出一系列应用,从体外诊断到各种目标的实时成像。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号