Abstract
Combinatorial methods enable the synthesis of chemical libraries on scales of millions to billions
of compounds, but the ability to efficiently screen and sequence such large libraries has remained
a major bottleneck for molecular discovery. We developed a novel technology for screening and
sequencing libraries of synthetic molecules of up to a billion compounds in size. This method
utilizes Fiber-optic Array Scanning Technology (FAST) to screen bead-based libraries of synthetic
compounds at a rate of 5 million compounds per minute (~83,000 Hz). This ultra-high-throughput
screening platform has been used to screen libraries of synthetic “self-readable” non-natural
polymers that can be sequenced at femtomole scale by chemical fragmentation and highresolution mass spectrometry. The versatility and throughput of the platform was demonstrated
by screening two libraries of non-natural polyamide polymers with sizes of 1.77M and 1B compounds against the protein targets K-Ras, asialoglycoprotein receptor (ASGPR), IL-6, IL-6
receptor and TNFα. Hits with nanomolar binding affinities were found against all targets,
including competitive inhibitors of K-Ras binding to Raf and functionally active uptake ligands for
ASGPR facilitating intracellular delivery.
Supplementary materials
Title
FAST screening platform SRI manuscript Supplemental
Description
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