Sign in
BioengineeringAngewandte Chemie International Edition
Peer-reviewed journal article

LASSO: versatile and selective biomolecule pulldown with combinatorial DNA-crosslinked polymers

Sarah K. SpeediD, Krishna GuptaiD, Yu‐Hsuan PengiD, Elisha KriegiD

Abstract

Current methods for sequence-selective biomolecule isolation suffer from high cost, off-target effects, and limited flexibility. Here, we introduce LASSO (crossLink-Assisted Sequence-Selective isOlation), a versatile platform using programmable polymer phase separation to capture biomolecules under native conditions. LASSO relies on combinatorial crosslinker libraries--diverse mixtures of DNA strands that collectively trigger the formation of highly swollen polymer agglomerates with near-zero background binding. We demonstrate >80% pulldown efficiency for diverse targets, including DNA, SARS-CoV-2 RNA, and human thrombin. LASSO provides 8-20x higher binding capacity (4 nmol/mg polymer) than commercial microbeads. In RNA-seq workflows, LASSO depleted ribosomal RNA with 86% efficiency while yielding up to 7x fewer off-target outliers (p<0.001) versus state-of-the-art magnetic beads (riboPOOLs) and RNase H (NEBNext) kits. Thrombin was captured via switchable aptamers with 92% efficiency, and a gentle release mechanism allowed the subsequent isolation of 72% enzymatically active proteins from the polymer. LASSOs cost-effectiveness ($0.96/sample vs. $46-$51 for commercial kits), long-term stability (7+ years), simple usage, and modularity position it to transform diagnostics, transcriptomics, and bionanotechnology workflows.

PDFDOI

02 /Specification & Classification

Click any tag to browse matching papers

Reproducibility ledger

Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.

Sign in to file a reproducibility report.