Abstract
CRISPR-Cas9-based forward genetic screens represent a powerful discovery platform to uncover genes regulating specific biological processes. This article describes a method for utilizing a freely available GlycoGene CRISPR library to knock out any gene participating in human glycosylation in arbitrary cell types. The end product is a stable GlycoGene CRISPR knockout cell library, where each cell contains one or more sgRNA and lacks corresponding function. The cell library can be screened using various lectin/antibody reagents. It can also be applied in functional assays to establish glycan structure-glycogene-glycopathway relationships. This is a powerful systems glycobiology strategy for dissecting glycosylation pathways and processes.
| Original language | English |
|---|---|
| Article number | e402 |
| Journal | Current Protocols in Microbiology |
| Volume | 2 |
| Issue number | 4 |
| DOIs | |
| State | Published - Apr 2022 |
Keywords
- CRISPR-Cas9
- glycogene
- glycosylation
- lectin
- pathway analysis
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