综述或非传感器论文 2012 非传感器论文

Recombinant antibodies and their use in biosensors.

Analytical and bioanalytical chemistry Zeng X, Shen Z, Mernaugh R
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组成图示

Recombinant antibodies and their use ... 传感器构成示意图

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传感器类型

综述或非传感器论文

检测对象

兔IgG(rabbit IgG,溶液/血清)、人CYP1B1(cytochrome P450 1B1,溶液)、曲妥珠单抗(Herceptin,人血清)、GD2阳性肿瘤细胞(GD2-positive cells,细胞悬液)、铀酰(UO2,环境水样)

检测原理

代表性压电免疫传感器中,重组scFv通过连接肽中的半胱氨酸或组氨酸与QCM金表面配位,或通过精氨酸与MUA/PSS负电荷层静电作用,实现高密度、正确取向固定。被测抗原与scFv可变区结合后,传感器表面质量增加;QCM压电晶体共振频率随表面质量增加而下降,频率变化(ΔF)与结合抗原质量及浓度相关。若使用蛋白A包被AuNP标记兔IgG的Fc区,纳米颗粒引入额外质量,形成信号放大,使检测灵敏度由纳摩尔级提高至皮摩尔/亚皮摩尔级。将QCM振荡频率从10 MHz提高到25 MHz可进一步提高约5倍灵敏度。多价scFv通过多个表位同时结合多价抗原或细胞表面受体,提高avidity和捕获效率。

检测灵敏度

原文未报告LOD、线性范围、灵敏度斜率或相关系数。

效应效果

综述报道的scFv压电免疫传感器抗干扰与选择性较好:A10B scFv-Cys表面非特异血清结合几乎不存在,完整IgG和Fab表面非特异结合较高;scFv-Cys表面抗原结合活性最高,覆盖约1.74±0.53×10^-10 mol cm^-2,比Fab'-SH高约10倍,比完整IgG高约35倍。scFv-RG3与负电荷SAM模板结合后,兔IgG结合活性较Fab传感器提高42倍;蛋白A-AuNP标记使灵敏度从纳摩尔级降至皮摩尔/亚皮摩尔级,25 MHz QCM较10 MHz提高5倍。双scFv同时结合策略可降低CYP1B1检测中BM-3等相似分子的假阳性。QCM可实时监测scFv固定量,有助于提高批间重现性,作者认为其适用于复杂生物样品中的疾病标志物检测。

传感器的构成

  • 换能器基底:石英晶体微天平(QCM)金电极(Au),提供压电换能表面和抗体固定位点
  • 表面修饰层:11-巯基十一烷酸(MUA)自组装单分子层(SAM)或聚苯乙烯磺酸钠(PSS)负电荷层,提供羧基或负电荷用于scFv定向固定
  • 识别元件:重组单链抗体片段(scFv),如A10B scFv-Cys、scFv-His、scFv-RG3,通过连接肽中的半胱氨酸、组氨酸或精氨酸实现表面自组装并保留抗原结合活性
  • 固定辅助层:链霉亲和素/亲和素(streptavidin/neutravidin)或Ni-NTA,用于固定生物素化scFv或6×His标签scFv
  • 信号标记物:蛋白A包被金纳米颗粒(Protein A-AuNP),结合兔IgG的Fc区以引入额外质量并增强QCM信号

中文摘要

低成本、无创免疫分析可用于快速检测人体疾病。免疫分析的灵敏度和特异性高度依赖于高亲和力、抗原特异性抗体。抗体由生物体产生,其质量及是否适合用于免疫分析难以通过人为干预直接确定或控制。然而,利用基因工程和重组抗体技术,获得高质量抗体的过程已被缩短和简化。传统上依赖动物免疫可能需要数月甚至更长时间获得的抗体,如今可在数周内以细菌、酵母或其他细胞中表达的重组抗体形式开发。多数免疫分析通常使用两种或多种抗体或抗体片段来检测作为疾病标志物的抗原;而无标记生物传感器,例如石英晶体微天平(QCM),仅需一种抗体。因此,与使用传统抗体和检测方法(如酶联免疫吸附试验,ELISA)相比,采用重组抗体和生物传感器可显著降低免疫分析设计与开发所需的成本和时间。与传统抗体不同,重组抗体可通过基因工程在生物传感器表面高密度、正确取向自组装,从而增强抗原结合活性,提高分析灵敏度、特异性和稳定性。此外,还可修饰生物传感器表面化学及物理电子性质,使免疫分析性能超越传统方法。本综述介绍了研究者用于开发高特异、高灵敏重组抗体生物传感器,以检测简单或复杂生物样品中抗原的一些技术。

英文摘要

Inexpensive, noninvasive immunoassays can be used to quickly detect disease in humans. Immunoassay sensitivity and specificity are decidedly dependent upon high-affinity, antigen-specific antibodies. Antibodies are produced biologically. As such, antibody quality and suitability for use in immunoassays cannot be readily determined or controlled by human intervention. However, the process through which high-quality antibodies can be obtained has been shortened and streamlined by use of genetic engineering and recombinant antibody techniques. Antibodies that traditionally take several months or more to produce when animals are used can now be developed in a few weeks as recombinant antibodies produced in bacteria, yeast, or other cell types. Typically most immunoassays use two or more antibodies or antibody fragments to detect antigens that are indicators of disease. However, a label-free biosensor, for example, a quartz-crystal microbalance (QCM) needs one antibody only. As such, the cost and time needed to design and develop an immunoassay can be substantially reduced if recombinant antibodies and biosensors are used rather than traditional antibody and assay (e.g. enzyme-linked immunosorbant assay, ELISA) methods. Unlike traditional antibodies, recombinant antibodies can be genetically engineered to self-assemble on biosensor surfaces, at high density, and correctly oriented to enhance antigen-binding activity and to increase assay sensitivity, specificity, and stability. Additionally, biosensor surface chemistry and physical and electronic properties can be modified to further increase immunoassay performance above and beyond that obtained by use of traditional methods. This review describes some of the techniques investigators have used to develop highly specific and sensitive, recombinant antibody-based biosensors for detection of antigens in simple or complex biological samples.