Nano-Polymers as Cas9 Inhibitors

Despite wide applications of CRISPR/Cas9 technology, effective approaches for CRISPR delivery with functional control are limited. In an attempt to develop a nanoscale CRSIPR/Cas9 delivery platform, we discovered that several biocompatible polymers, including polymalic acid (PMLA), polyglutamic acid (PGA), and polyaspartic acid (PLD), when conjugated with a trileucine (LLL) moiety, can effectively inhibit Cas9 nuclease function. The Cas9 inhibition by those polymers is dose-dependent, with varying efficiency to achieve 100% inhibition. Further biophysical studies revealed that PMLA-LLL directly binds the Cas9 protein, resulting in a substantial decrease in Cas9/sgRNA binding affinity. Transmission electron microscopy and molecular docking were performed to provide a possible binding mechanism for PMLA-LLL to interact with Cas9. This work identified a new class of Cas9 inhibitor in nano-polymer form. These biodegradable polymers may serve as novel Cas9 delivery vehicles with a potential to enhance the precision of Cas9-mediated gene editing.

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Publication Details

Journal
Polymers
Published
2025-02-05
DOI
https://doi.org/10.3390/polym17030417
Primary Topic
CRISPR and Genetic Engineering
Type
article
Field-Weighted Citation Impact
0.00

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article

Nano-Polymers as Cas9 Inhibitors

Ramachandran Murali, Keith L. Black, Tao Sun, Avradip Chatterjee et al.
Polymers
CRISPR and Genetic Engineering
article

Nano-Polymers as Cas9 Inhibitors

Ramachandran Murali, Keith L. Black, Tao Sun, Avradip Chatterjee, Oksana Chepurna, Hong Ding, Yuan‐Qing Li
article en

Abstract

Despite wide applications of CRISPR/Cas9 technology, effective approaches for CRISPR delivery with functional control are limited. In an attempt to develop a nanoscale CRSIPR/Cas9 delivery platform, we discovered that several biocompatible polymers, including polymalic acid (PMLA), polyglutamic acid (PGA), and polyaspartic acid (PLD), when conjugated with a trileucine (LLL) moiety, can effectively inhibit Cas9 nuclease function. The Cas9 inhibition by those polymers is dose-dependent, with varying efficiency to achieve 100% inhibition. Further biophysical studies revealed that PMLA-LLL directly binds the Cas9 protein, resulting in a substantial decrease in Cas9/sgRNA binding affinity. Transmission electron microscopy and molecular docking were performed to provide a possible binding mechanism for PMLA-LLL to interact with Cas9. This work identified a new class of Cas9 inhibitor in nano-polymer form. These biodegradable polymers may serve as novel Cas9 delivery vehicles with a potential to enhance the precision of Cas9-mediated gene editing.

PolymersVol. 17(3)
Shenyang Pharmaceutical University (CN), Cedars-Sinai Medical Center (US), Chinese Academy of Sciences (CN), Shanghai Institutes for Biological Sciences (CN)
University of California, Los Angeles, Clinical and Translational Science Institute, University of California, Los Angeles, California NanoSystems Institute
Affordable and clean energy
Openalex Percentile: Top 98%
CRISPR and Genetic Engineering
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