Engineered membrane protein antigens successfully induce antibodies against extracellular regions of claudin-5.

ABSTRACT: The production of antibodies against the extracellular regions (ECR) of multispanning membrane proteins is notoriously difficult because of the low productivity and immunogenicity of membrane proteins due to their complex structure and highly conserved sequences among species. Here, we introduce a new method to generate ECR-binding antibodies utilizing engineered liposomal immunogen prepared using a wheat cell-free protein synthesis system. We used claudin-5 (CLDN-5) as the target antigen, which is a notoriously difficult to produce and poorly immunogenic membrane protein with two highly conserved extracellular loops. We drastically improved the productivity of CLDN-5 in the cell-free system after suppressing and normalizing mRNA GC content. To overcome its low immunogenicity, two engineer

SUBMITTER: Hashimoto Y 

PROVIDER: S-EPMC5976803 | biostudies-literature | 2018 May

REPOSITORIES: biostudies-literature