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用于高效递送 CRISPR/Cas9 和 mRNA 的高发光氮锌掺杂碳点。

Highly Photoluminescent Nitrogen- and Zinc-Doped Carbon Dots for Efficient Delivery of CRISPR/Cas9 and mRNA.

机构信息

Cellular and Molecular Research Center, Iran University of Medical Sciences, Tehran 1449614535, Iran.

Department of Medical Nanotechnology, Faculty of Advanced Technologies in Medicine, Iran University of Medical Sciences, Tehran 1449614535, Iran.

出版信息

Bioconjug Chem. 2021 Aug 18;32(8):1875-1887. doi: 10.1021/acs.bioconjchem.1c00309. Epub 2021 Jul 19.

Abstract

Safe and efficient delivery of CRISPR/Cas9 systems is still a challenge. Here we report the development of fluorescent nitrogen- and zinc-doped carbon dots (N-Zn-doped CDs) using one-step microwave-aided pyrolysis based on citric acid, branched PEI, and different zinc salts. These versatile nanovectors with a quantum yield of around 60% could not only transfect large CRISPR plasmids (∼9 kb) with higher efficiency (80%) compared to PEI and lipofectamine 2000 (Lipo 2K), but they also delivered mRNA into HEK 293T cells with the efficiency 20 times greater than and equal to that of PEI and Lipo 2K, respectively. Unlike PEI, N-Zn-doped CDs exhibited good transfection efficiency even at low plasmid doses and in the presence of 10% fetal bovine serum (FBS). Moreover, these nanovectors demonstrated excellent efficiency in GFP gene disruption by transferring plasmid encoding Cas9 and sgRNA targeting GFP as well as Cas9/sgRNA ribonucleoproteins into HEK 293T-GFP cells. Hence, N-Zn-doped CDs with remarkable photoluminescence properties and high transfection efficiency in the delivery of both CRISPR complexes and mRNA provide a promising platform for developing safe, efficient, and traceable delivery systems for biological research.

摘要

CRISPR/Cas9 系统的安全有效递送仍然是一个挑战。在这里,我们报告了使用基于柠檬酸、支化 PEI 和不同锌盐的一步微波辅助热解法开发荧光氮锌掺杂碳点 (N-Zn-doped CDs)。这些多功能纳米载体的量子产率约为 60%,与 PEI 和脂质体 2000 (Lipo 2K) 相比,不仅能够更有效地转染大的 CRISPR 质粒(约 9 kb)(效率为 80%),而且能够将 mRNA 递送入 HEK 293T 细胞,效率分别比 PEI 和 Lipo 2K 高 20 倍和 20 倍以上。与 PEI 不同,N-Zn-doped CDs 即使在低质粒剂量和存在 10%胎牛血清 (FBS) 的情况下,也表现出良好的转染效率。此外,这些纳米载体在 GFP 基因敲除方面表现出优异的效率,将编码 Cas9 和 sgRNA 靶向 GFP 的质粒以及 Cas9/sgRNA 核糖核蛋白转染到 HEK 293T-GFP 细胞中。因此,具有显著光致发光性能和高转染效率的 N-Zn-doped CDs 在递送 CRISPR 复合物和 mRNA 方面提供了一个有前途的平台,用于开发安全、有效和可追踪的生物研究递送系统。

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