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Bacterial Protoplast-Derived Nanovesicles Carrying CRISPR Cas9 Tools Efficiently Re-educate Tumor-Associated Macrophages for Cancer Immunotherapy

ABSTRACT: we developed an in vivo CRISPR-Cas9 genome editing system that targets tumor-associated macrophages (TAMs) via bacterial protoplast-derived nanovesicles (NVs) decorated with a pH-responsive PEG conjugated polymer and galactosamine-conjugated ligand

ORGANISM(S): Escherichia Coli Bl21(de3)

SUBMITTER: Junfeng Zhang

PROVIDER: PXD045507 | iProX | Wed Sep 20 00:00:00 BST 2023

REPOSITORIES: iProX

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Bacterial protoplast-derived nanovesicles carrying CRISPR-Cas9 tools re-educate tumor-associated macrophages for enhanced cancer immunotherapy.

Zhao Mingming M Cheng Xiaohui X Shao Pingwen P Dong Yao Y Wu Yongjie Y Xiao Lin L Cui Zhiying Z Sun Xuedi X Gao Chuancheng C Chen Jiangning J Huang Zhen Z Zhang Junfeng J

Nature communications 20240131 1

The CRISPR-Cas9 system offers substantial potential for cancer therapy by enabling precise manipulation of key genes involved in tumorigenesis and immune response. Despite its promise, the system faces critical challenges, including the preservation of cell viability post-editing and ensuring safe in vivo delivery. To address these issues, this study develops an in vivo CRISPR-Cas9 system targeting tumor-associated macrophages (TAMs). We employ bacterial protoplast-derived nanovesicles (NVs) mod ...[more]

PMID: 38296939

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Genome-wide specificity of genome editing by both CRISPR-Cas9 and TALEN in the model plant Physcomitrium patens

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2022-03-03 | E-MTAB-11497 | biostudies-arrayexpress

A multi-functional AAV-CRISPR-Cas9 and its host response

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Targeted DNA-seq of Human HepG2 cells following editing with CRISPR/Cas9

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Amplicon-Screening of genomic DNA regions of mutants in the Exon5 R175 position of TP53 in HCT116 cells generated via CRISPR editing

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