Lin Baochuan, Delehanty James B
United States Naval Research Laboratory, Center for Bio/Molecular Science and Engineering, Washington, DC, USA.
Methods Mol Biol. 2011;706:119-37. doi: 10.1007/978-1-61737-970-3_10.
Transfected cell microarrays, arrays of cells expressing defined cDNAs, are promising technologies that can enable the functional analysis of many proteins in parallel. This technique has been adapted for the comparative functional analysis of single-chain antibodies (scFvs) and to facilitate the screening and characterization of these antibodies for their use in diagnostic and therapeutic applications. In this method, membrane-targeting expression vectors encoding scFvs are mixed with transfection reagents and are deposited at high density onto a microscope slide. Adherent mammalian cells are subsequently added to the printed array. Upon attachment to the substrate, the cells take up the plasmid DNA and express the particular protein encoded at each location. The result is an array whose features are micrometer-sized clusters of cells expressing defined genes. This approach provides for the high-throughput functional analysis of many different proteins in parallel and can be considerably more informative and cost-effective relative to more traditional protein expression techniques.
转染细胞微阵列,即表达特定cDNA的细胞阵列,是很有前景的技术,能够并行实现对多种蛋白质的功能分析。这项技术已被用于单链抗体(scFv)的比较功能分析,并有助于筛选和鉴定这些抗体,以用于诊断和治疗应用。在该方法中,将编码scFv的膜靶向表达载体与转染试剂混合,并高密度沉积到显微镜载玻片上。随后将贴壁哺乳动物细胞添加到印制的阵列上。细胞附着于底物后,会摄取质粒DNA并表达每个位置编码的特定蛋白质。结果得到一个阵列,其特征是表达特定基因的微米级细胞簇。这种方法能够并行对多种不同蛋白质进行高通量功能分析,相对于更传统的蛋白质表达技术,可能更具信息性且更具成本效益。