Related Experiment Video
Updated: Aug 17, 2025

A Protocol for Functional Assessment of Whole-Protein Saturation Mutagenesis Libraries Utilizing High-Throughput Sequencing
Published on: July 3, 2016
Streamlined high-throughput cloning protocol to generate arrayed mutant libraries
Kerry T Sun1, Tark S Patel1, Justin Kim1
1Department of Biochemistry, University of Alberta, Edmonton, AB, Canada.
Abstract:
Large-scale, site-directed mutagenesis enables rapid characterization of the biochemical and biological properties of proteins. Here, we present a cost-effective and adaptable cloning pipeline to generate arrayed gene libraries for a construct of interest. We detail steps to use an open access web app to automate the design of mutagenesis primers optimized for our cloning protocols in a 96-well plate format. The protocol allows most molecular biology labs to clone 96 mutants (from PCR to sequence ready plasmid) in 3 days.

