Love J Christopher, Ronan Jehnna L, Grotenbreg Gijsbert M, van der Veen Annemarthe G, Ploegh Hidde L
Whitehead Institute for Biomedical Research, 9 Cambridge Center, Cambridge, Massachusetts 02142, USA.
Nat Biotechnol. 2006 Jun;24(6):703-7. doi: 10.1038/nbt1210. Epub 2006 May 14.
Monoclonal antibodies that recognize specific antigens of interest are used as therapeutic agents and as tools for biomedical research. Discovering a single monoclonal antibody requires retrieval of an individual hybridoma from polyclonal mixtures of cells producing antibodies with a variety of specificities. The time required to isolate hybridomas by a limiting serial-dilution, however, has restricted the diversity and breadth of available antibodies. Here we present a soft lithographic method based on intaglio printing to generate microarrays comprising the secreted products of single cells. These engraved arrays enable a rapid (<12 h) and high-throughput (>100,000 individual cells) system for identification, recovery and clonal expansion of cells producing antigen-specific antibodies. This method can be adapted, in principle, to detect any secreted product in a multiplexed manner.
识别特定目标抗原的单克隆抗体被用作治疗剂和生物医学研究工具。发现一种单克隆抗体需要从产生具有多种特异性抗体的细胞多克隆混合物中获取单个杂交瘤。然而,通过有限系列稀释分离杂交瘤所需的时间限制了可用抗体的多样性和广度。在此,我们展示一种基于凹版印刷的软光刻方法,以生成包含单细胞分泌产物的微阵列。这些刻蚀阵列实现了一个快速(<12小时)且高通量(>100,000个单个细胞)的系统,用于鉴定、回收和克隆扩增产生抗原特异性抗体的细胞。原则上,这种方法可适用于以多重方式检测任何分泌产物。