Abstract
AbstractIdentification of functional elements for a protein of interest is important for achieving a mechanistic understanding. However, it remains cumbersome to assess each and every amino acid of a given protein in relevance to its functional significance. Here, we report a strategy, PArsing fragmented DNA Sequences from CRISPR Tiling MUtagenesis Screening (PASTMUS), which provides a streamlined workflow and a bioinformatics pipeline to identify critical amino acids of proteins in their native biological contexts. Using this approach, we map six proteins—three bacterial toxin receptors and three cancer drug targets, and acquire their corresponding functional maps at amino acid resolution.
Funder
Key Programme
Natural Science Foundation of Tianjin Municipal Science and Technology Commission
National Major Science and Technology Projects of China
Young Scientists Fund
Publisher
Springer Science and Business Media LLC
Cited by
6 articles.
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