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基于细胞穿透肽的三重纳米复合物实现莱茵衣藻中高效的核基因递送

Cell-Penetrating Peptide-Based Triple Nanocomplex Enables Efficient Nuclear Gene Delivery in Chlamydomonas reinhardtii.

作者信息

Sim Eun Jeong, Tran Quynh-Giao, Lee Yu Rim, Le Trang Thi, Yoon Hyang Ran, Choi Dong-Yun, Cho Dae-Hyun, Yun Jin-Ho, Il Choi Hong, Kim Hee-Sik, Lee Yong Jae

机构信息

Cell Factory Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Daejeon, Republic of Korea.

Department of Environmental Biotechnology, KRIBB School of Biotechnology, University of Science and Technology (UST), Daejeon, Republic of Korea.

出版信息

Biotechnol Bioeng. 2025 Aug;122(8):2218-2227. doi: 10.1002/bit.29019. Epub 2025 May 8.

Abstract

Microalgae are a promising solution for mitigating climate change due to their ability to capture greenhouse gases and produce renewable materials. However, their effective application is often hindered by barriers that necessitate advances in genetic engineering to improve photosynthesis and productivity. One major obstacle is the microalgal cell wall, which complicates the delivery of genetic material into these organisms. To address these challenges, we developed a novel triple nanocomplex system integrating cell-penetrating peptides (CPPs), nuclear localization signal (NLS) peptides, and plasmid DNA. This system allows simple preparation while achieving efficient nuclear translocation of plasmid DNA. We evaluated two CPPs, pVEC-ORI and pVEC-R6A, for their efficacy in facilitating intracellular transfer of DNA into wild-type Chlamydomonas reinhardtii cells. Notably, pVEC-R6A demonstrated a 6.88-fold increase in efficiency compared to pVEC-ORI, despite the presence of thick cell walls. The optimal CPP:DNA ratio for stable nanocomplex formation was determined to be 5:1 for pVEC-ORI and 10:1 for pVEC-R6A. By incorporating the simian virus 40 (SV40) NLS into CPP/DNA nanocomplexes, we successfully directed the localization of plasmid DNA into the nucleus. Our findings indicate that this simple and efficient DNA delivery system has significant potential as a tool to advance microalgal synthetic biology.

摘要

微藻因其具有捕获温室气体和生产可再生材料的能力,是缓解气候变化的一个有前景的解决方案。然而,它们的有效应用常常受到阻碍,这些阻碍需要基因工程取得进展以改善光合作用和生产力。一个主要障碍是微藻细胞壁,它使遗传物质导入这些生物体的过程变得复杂。为应对这些挑战,我们开发了一种新型的三联纳米复合系统,该系统整合了细胞穿透肽(CPPs)、核定位信号(NLS)肽和质粒DNA。这个系统制备简单,同时能实现质粒DNA的高效核转运。我们评估了两种CPPs,即pVEC-ORI和pVEC-R6A,它们促进DNA细胞内转移到野生型莱茵衣藻细胞中的效果。值得注意的是,尽管存在厚厚的细胞壁,pVEC-R6A的效率相比pVEC-ORI提高了6.88倍。确定形成稳定纳米复合物的最佳CPP与DNA比例,对于pVEC-ORI为5:1,对于pVEC-R6A为10:1。通过将猴病毒40(SV40)NLS整合到CPP/DNA纳米复合物中,我们成功地将质粒DNA的定位引导到细胞核中。我们的研究结果表明,这种简单高效的DNA递送系统作为推进微藻合成生物学的工具具有巨大潜力。

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