Diagnostic nanoprobes based on the conjugates of quantum dots and single-domain antibodies for cancer biomarkers detection in immunohistochemistry and flow cytometry

A. Sukhanova, J. Millot, M. Pluot, J. Cohen, I. Nabiev
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引用次数: 1

Abstract

Monoclonal antibodies (mAbs) are often too big for the nanoparticle targeting purpose and the conditions used for their conjugation provide nanoprobes with irregular orientation of mAbs on the surface of nanoparticle. Here, we are reviewing our recent publications reporting on ultra-small nanoprobes engineered through oriented conjugation of quantum dots (QDs) with 13-kDa single-domain antibodies (sdAbs) derived from llama and produced in E. coli. Developed nanoprobes with hydrodynamic diameter below 12 nm contain four homogeneously oriented copies of sdAbs on the surface of each QD. They demonstrated excellent specificity and sensitivity for the quantitative detection of rare biomarker-expressing cells using flow cytometry. The higher diffusibility of sdAbs enables immunohistochemical analysis of thick tissues not accessible to mAbs. The data shows that sdAbs-QD conjugates lead to biopsy tissue labelling displaying an equivalent or even better quality than that obtained with gold standard immunohistochemical diagnostics. Developed sdAbs-QD nanoprobes should find numerous applications in multiplexed high-throughput diagnostics and FRET-based detection platforms.
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基于量子点和单域抗体偶联物的诊断纳米探针在免疫组织化学和流式细胞术中检测癌症生物标志物
单克隆抗体(mab)对于纳米颗粒的靶向作用来说通常太大,并且它们的偶联条件使得纳米探针在纳米颗粒表面具有不规则的单克隆抗体取向。在这里,我们回顾了我们最近发表的关于量子点(QDs)与13kda单域抗体(sabs)定向偶联的超小型纳米探针的报道,这些抗体来源于羊驼,并在大肠杆菌中产生。所开发的水动力直径小于12 nm的纳米探针在每个量子点表面含有4个均匀取向的单克隆抗体拷贝。它们在流式细胞术中对表达罕见生物标志物的细胞进行定量检测时表现出极好的特异性和敏感性。单克隆抗体的高扩散性使得单克隆抗体无法对厚组织进行免疫组化分析。数据显示,sabs - qd偶联物导致活检组织标记显示出与金标准免疫组织化学诊断获得的相同甚至更好的质量。开发的sds - qd纳米探针应该在多路高通量诊断和基于fret的检测平台中找到许多应用。
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