Flow-Cell-Based Technology for Massively Parallel Characterization of Base-Modified DNA Aptamers

Aptamers incorporating chemically modified bases can achieve superior affinity and specificity compared to natural aptamers, but their characterization remains a labor-intensive, low-throughput task. Here, we describe the non-natural aptamer array (N2A2) system, in which a minimally modified Illumina MiSeq instrument is used for the high-throughput generation and characterization of large libraries of base-modified DNA aptamer candidates based on both target binding and specificity. We first demonstrate the capability to screen multiple different base modifications to identify the optimal chemistry for high-affinity target binding. We next use N2A2 to generate aptamers that can maintain excellent specificity even in complex samples, with equally strong target affinity in both buffer and diluted human serum. For both aptamers, affinity was formally calculated with gold-standard binding assays. Given that N2A2 requires only minor mechanical modifications to the MiSeq, we believe that N2A2 offers a broadly accessible tool for generating high-quality affinity reagents for diverse applications.

Automated summary

Aptamers incorporating chemically modified bases can achieve superior affinity and specificity compared to natural aptamers. The non-natural aptamer array (N2A2) system offers a high-throughput method for generating and characterizing large libraries of base-modified DNA aptamers. The N2A2 system provides a broadly accessible tool for generating high-quality affinity reagents for diverse applications.