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Quantification of Protein Interaction Network Dynamics using Multiplexed Co-Immunoprecipitation
Published on: August 21, 2019
Amplicon/Protein Bead Display enables quantitative in vitro biochemistry at scale
Daria R Passow1, Anvita Gupta2, Samuel Thompson3,4
1Biophysics Program, Stanford University, Stanford, CA 94305, USA.
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Scalable methods for producing and characterizing protein libraries are essential for generating standardized datasets needed to train models linking sequence to function. Here, we present Amplicon/Protein Bead Display (APB-Display), which expresses and purifies >100,000 protein variants in vitro in 1 day. APB-Display uses particle-templated emulsification to generate libraries of hydrogel beads that covalently display many copies of a given protein variant and its encoding DNA. By incubating beads with fluorescently-labeled ligands, sorting, and sequencing to generate titration curves (APB-TiteSeq), we simultaneously quantified expression levels and binding affinities for >18,000 FLAG epitope variants interacting with M2 anti-FLAG antibody in 3 days, revealing chemistry-dependent epistasis between positions 4 and 5. Single-concentration binding measurements (APB-SortSeq) paired with neural network denoising further returned quantitative affinities for >88,000 variants. APB-Display requires only standard laboratory equipment and access to a FACS sorter, providing an accessible platform for quantitative in vitro biochemistry at scale.

