Department of Chemistry, Oakland University, 2200 Squirrel Road, Rochester, MI 48309, USA.
Anal Bioanal Chem. 2012 Apr;402(10):3027-38. doi: 10.1007/s00216-011-5569-z. Epub 2011 Dec 13.
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.
廉价、非侵入性的免疫分析可以用于快速检测人类疾病。免疫分析的敏感性和特异性取决于高亲和力、抗原特异性的抗体。抗体是通过生物途径产生的。因此,抗体的质量和在免疫分析中的适用性不能通过人为干预来轻易确定或控制。然而,通过使用基因工程和重组抗体技术,已经缩短并简化了获得高质量抗体的过程。使用动物生产抗体通常需要几个月或更长时间,但现在可以通过在细菌、酵母或其他细胞类型中生产重组抗体,在几周内开发出来。通常,大多数免疫分析使用两种或更多的抗体或抗体片段来检测作为疾病指标的抗原。然而,例如无标记生物传感器(石英晶体微天平,QCM)仅需要一种抗体。因此,如果使用重组抗体和生物传感器而不是传统的抗体和分析(例如酶联免疫吸附分析,ELISA)方法,可以大大降低设计和开发免疫分析所需的成本和时间。与传统抗体不同,重组抗体可以通过基因工程设计,使其在生物传感器表面上自组装,形成高密度、正确取向的结构,从而增强抗原结合活性,提高分析的灵敏度、特异性和稳定性。此外,可以修饰生物传感器表面的化学性质以及物理和电子特性,以进一步提高免疫分析的性能,超越使用传统方法获得的性能。本综述描述了研究人员用于开发基于重组抗体的高特异性和高灵敏度生物传感器以检测简单或复杂生物样本中抗原的一些技术。