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使用封装 RNA 的脂质纳米颗粒递送至实体瘤中的 CRISPR/dCas9 系统用于表观遗传学编辑的方案。

Protocol for Delivery of CRISPR/dCas9 Systems for Epigenetic Editing into Solid Tumors Using Lipid Nanoparticles Encapsulating RNA.

机构信息

Cancer Epigenetics Group, Harry Perkins Institute of Medical Research, Perth, WA, Australia.

Centre for Medical Research, University of Western Australia, Perth, WA, Australia.

出版信息

Methods Mol Biol. 2024;2842:267-287. doi: 10.1007/978-1-0716-4051-7_14.

Abstract

Genome editing tools, particularly the Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR) systems (e.g., CRISPR/Cas9), and their repurposing into epigenetic editing platforms, offer enormous potential as safe and customizable therapies for cancer. Specifically, various transcriptional abnormalities in human malignancies, such as silencing of tumor suppressors and ectopic re-expression of oncogenes, have been successfully targeted with virtually no off-target effects using CRISPR activation and repression systems. In these systems, the nuclease-deactivated Cas9 protein (dCas9) is fused to one or more domains inducing selective activation or repression of the targeted genes. Despite these advances, the efficient in vivo delivery of these molecules into the target cancer cells represents a critical barrier to accomplishing translation into a clinical therapy setting for cancer. Major obstacles include the large size of dCas9 fusion proteins, the necessity of multimodal delivery of protein and gRNAs, and the potential of these formulations to elicit detrimental immune responses.In this context, viral methods for delivering CRISPR face several limitations, such as the packaging capacity of the viral genome, the potential for integration of the nucleic acids into the host cells genome, and immunogenicity of viral proteins, posing serious safety concerns. The rapid development of mRNA vaccines in response to the COVID-19 pandemic has rekindled interest in mRNA-based approaches for CRISPR/dCas9 delivery. Simultaneously, due to their high loading capacity, scalability, customizable surface modification for cell targeting, and low immunogenicity, lipid nanoparticles (LNPs) have been widely explored as nonviral vectors. In this chapter, we first describe the design of optimized dCas9-effector mRNAs and gRNAs for epigenetic editing. We outline formulations of LNPs suitable for dCas9 mRNA delivery. Additionally, we provide a protocol for the co-encapsulation of the dCas9-effector mRNAs and gRNA into these LNPs, along with detailed methods for delivering these formulations to both cell lines (in vitro) and mouse models of breast cancer (in vivo).

摘要

基因组编辑工具,特别是簇状规律间隔短回文重复序列(CRISPR)系统(例如,CRISPR/Cas9)及其重新用于表观遗传编辑平台,为癌症的安全和定制疗法提供了巨大的潜力。具体来说,人类恶性肿瘤中的各种转录异常,如肿瘤抑制因子的沉默和癌基因的异位重新表达,已经使用 CRISPR 激活和抑制系统成功靶向,几乎没有脱靶效应。在这些系统中,核酸酶失活的 Cas9 蛋白(dCas9)与一个或多个诱导靶向基因选择性激活或抑制的结构域融合。尽管取得了这些进展,但将这些分子有效地递送到靶癌细胞中仍然是将其转化为癌症临床治疗的关键障碍。主要障碍包括 dCas9 融合蛋白的体积较大、蛋白和 gRNA 的多模态递送的必要性以及这些制剂引发有害免疫反应的潜力。在这种情况下,用于递送 CRISPR 的病毒方法存在一些限制,例如病毒基因组的包装容量、核酸整合到宿主细胞基因组的可能性以及病毒蛋白的免疫原性,这些都带来了严重的安全问题。mRNA 疫苗在应对 COVID-19 大流行方面的快速发展重新激发了人们对基于 mRNA 的 CRISPR/dCas9 递送方法的兴趣。同时,由于其高载药量、可扩展性、针对细胞靶向的可定制表面修饰和低免疫原性,脂质纳米颗粒(LNP)已被广泛探索作为非病毒载体。在本章中,我们首先描述了用于表观遗传编辑的优化 dCas9 效应物 mRNA 和 gRNA 的设计。我们概述了适合 dCas9 mRNA 递送的 LNP 制剂。此外,我们提供了一种将 dCas9 效应物 mRNA 和 gRNA 共包封到这些 LNP 中的方案,以及将这些制剂递送到细胞系(体外)和乳腺癌小鼠模型(体内)的详细方法。

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