Related Experiment Video
Updated: May 26, 2026

Enhanced Genome Editing with Cas9 Ribonucleoprotein in Diverse Cells and Organisms
Published on: May 25, 2018
PrEditR: A protein-centric platform for CRISPR-mediated base editor sgRNA design
Felipe Vasquez-Castro1,2, Leonardo D Sanchez Solis1, Samuel A Myers1,3,4,5
1Laboratory for Immunochemical Circuits, La Jolla Institute for Immunology, La Jolla, CA 92037, United States of America.
Motivation:
Post-translational modifications (PTMs) are critical to protein function, yet the function of most known modification sites remains uncharacterized. CRISPR-mediated phenotypic screens using base editors offer a powerful approach to dissecting PTM function at scale. However, existing sgRNA design tools for base editing applications are DNA-centric and lack the throughput required to integrate seamlessly with mass-spectrometry-based proteomics experimental outputs.
Results:
We introduce protein editing in R, PrEditR, an open-source, protein-centric tool for high-throughput sgRNA design for custom base editor screens. PrEditR enables users to designate specific amino acid residues in proteins and design protospacer sequences to target the endogenous gene to install missense mutations via base editors.
Availability And Implementation:
PrEditR is available on GitHub and Docker Hub.
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