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Detection of Antibodies in Blood Plasma Using Bioluminescent Sensor Proteins and a Smartphone

机译:使用生物发光传感器蛋白和智能手机检测血浆中的抗体

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摘要

Antibody detection is of fundamental importance in many diagnostic and bioanalytical assays, yet current detection techniques tend to be laborious and/or expensive. We present a new sensor platform (LUMABS) based on bioluminescence resonance energy transfer (BRET) that allows detection of antibodies directly in solution using a smartphone as the sole piece of equipment. LUMABS are single-protein sensors that consist of the blue-light emitting luciferase NanoLuc connected via a semiflexible linker to the green fluorescent acceptor protein mNeonGreen, which are kept close together using helper domains. Binding of an antibody to epitope sequences flanking the linker disrupts the interaction between the helper domains, resulting in a large decrease in BRET efficiency. The resulting change in color of the emitted light from, green-blue to blue can be detected directly in blood plasma, even at picomolar concentrations of antibody. Moreover, the modular architecture of LUMABS allows changing of target specificity by simple exchange of epitope sequences, as demonstrated here for antibodies against HIV1-p17, hemagglutinin (HA), and dengue virus type I. The combination of sensitive ratiometric bioluminescent detection and the intrinsic modularity of the LUMABS design provides an attractive generic platform for point-of-care antibody detection that avoids the complex liquid handling steps associated with conventional immunoassays.
机译:在许多诊断和生物分析测定中,抗体检测至关重要,但是目前的检测技术往往很费力和/或昂贵。我们提出了一种基于生物发光共振能量转移(BRET)的新传感器平台(LUMABS),该平台允许使用智能手机作为唯一设备直接在溶液中检测抗体。 LUMABS是一种单蛋白传感器,由通过半柔性接头连接到绿色荧光受体蛋白mNeonGreen的发蓝光的荧光素酶NanoLuc组成,后者通过辅助结构域保持紧密连接。抗体与连接子侧翼的表位序列的结合破坏了辅助结构域之间的相互作用,导致BRET效率大大降低。即使在皮摩尔浓度的抗体下,也可以直接在血浆中检测出从绿色蓝色到蓝色的发射光颜色变化。此外,LUMABS的模块化体系结构允许通过简单的表位序列交换来改变靶标特异性,如此处针对HIV1-p17,血凝素(HA)和I型登革热病毒的抗体所示。 LUMABS设计的模块性为即时检测抗体提供了一个有吸引力的通用平台,从而避免了与常规免疫测定相关的复杂液体处理步骤。

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