Related Experiment Video
Updated: Mar 28, 2026

09:51
Enhanced Genome Editing with Cas9 Ribonucleoprotein in Diverse Cells and Organisms
Published on: May 25, 2018
36.3K
Protocol for enhancing Cas9 efficiency and fidelity through structure-guided phosphate-locking loop engineering
Meiying Yang1, Guanqiao Chen2, Ji Xiao2
1Department of Gynaecology, Guilin People' S Hospital, 12 Wenming Road, Xiangshan District, Guilin, Guangxi 541002, China.
STAR Protocols
|March 26, 2026
Summary
This study introduces a method for improving CRISPR-Cas9 gene editing tools by engineering the phosphate-locking loop (PLL). This structure-guided approach enhances the efficiency and precision of Cas9 for better DNA targeting.
Area of Science:
- Biochemistry
- Molecular Biology
- Gene Editing Technologies
Background:
- The phosphate-locking loop (PLL) is crucial for stabilizing Cas9-DNA interactions in CRISPR systems.
- Optimizing Cas9 efficiency and specificity is essential for advancing gene editing applications.
- Targeting the PLL offers a promising strategy for Cas9 enhancement.
Purpose of the Study:
- To present a protocol for structure-guided engineering of the Cas9 phosphate-locking loop (PLL).
- To enhance the efficiency and fidelity of Cas9 gene editing.
- To provide a generalizable framework for Cas9 ortholog engineering.
Main Methods:
- Sequence alignment and structural analysis to identify PLL engineering targets.
- Inverse PCR for constructing Cas9 variants with modified PLLs.
- Amplicon sequencing to evaluate gene editing efficiency.
- Genome-wide Unbiased Identification of DSBs Evaluated by sequencing (GUIDE-seq) to assess specificity.
Main Results:
- Demonstrated a protocol for structure-guided PLL engineering in Cas9.
- Successfully enhanced Cas9 efficiency and fidelity through PLL modifications.
- Validated the protocol's generalizability across different Cas9 orthologs.
Conclusions:
- Structure-guided engineering of the PLL is an effective strategy for improving Cas9 performance.
- The presented protocol offers a robust framework for developing enhanced Cas9 variants.
- This work facilitates the development of more precise and efficient gene editing tools.
Related Concept Videos
Conservative Site-specific Recombination and Phase Variation
7.3K
Because the DNA segments are cut and reorganized in a direction-specific manner, site-specific recombination has emerged as an efficient genetic engineering technique. Flippase and Cyclization recombinases or Flp and Cre, respectively, are two members of the tyrosine recombinase family derived from bacteriophages, that are used to mediate site-specific DNA insertions, deletions, and targeted expression of proteins in mammalian cell lines.
The recognition sites for Cre recombinase called LoxP...
The recognition sites for Cre recombinase called LoxP...
7.3K
CRISPR/Cas9 Genome Editing
2.6K
The CRISPR-Cas system serves as a bacterial defense mechanism against invading genetic elements such as viruses and plasmids, forming the foundation for its adaptation as a powerful genome-editing tool. Originally discovered in prokaryotes, this system has been repurposed to revolutionize genetic engineering across a wide range of organisms, including plants, animals, and humans. The core component, Cas9, is an endonuclease derived from Streptococcus pyogenes, capable of introducing...
2.6K
CRISPR
59.0K
Genome editing technologies allow scientists to modify an organism’s DNA via the addition, removal, or rearrangement of genetic material at specific genomic locations. These types of techniques could potentially be used to cure genetic disorders such as hemophilia and sickle cell anemia. One popular and widely used DNA-editing research tool that could lead to safe and effective cures for genetic disorders is the CRISPR-Cas9 system. CRISPR-Cas9 stands for Clustered Regularly Interspaced...
59.0K

