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Construction of peptide/plasmid DNA complexes for plant gene transfection via the basic leucine zipper domain
Polymer Journal ( IF 2.8 ) Pub Date : 2024-03-05 , DOI: 10.1038/s41428-024-00901-0
Kota Nomura , Seiya Fujita , Yuki Shimatani , Taichi Kurita , Chonprakun Thagun , Naoya Abe , Kazusato Oikawa , Kousuke Tsuchiya , Hirotaka Uji , Keiji Numata

An important method for plant genetic modification is using peptide/pDNA complexes to transfer genes into plant cells. With conventional carrier peptides, the peptide sequence must contain a high amount of cationic amino acids to condense and introduce pDNA. As a result, the dissociation of pDNA from the complex is inefficient, often causing problems. Herein, we designed a new peptide carrier that mimics the basic leucine zipper (bZIP) domain of DNA-binding proteins, in which (LU)4 is the leucine zipper motif and (KUA)3 is the basic DNA-binding and cell-penetrating motif (U = α-aminoisobutyric acid). After (KUA)3-(LU)4 peptide was mixed with pDNA, DNA molecules were condensed to form nanoparticles of approximately 130 nm. Furthermore, when complexes of (KUA)3-(LU)4 peptide and pDNA were introduced into the leaves of Arabidopsis thaliana (A. thaliana), expression of the reporter protein was detected in the plant cells. Thus, (KUA)3-(LU)4 peptide that mimics the bZIP domain is a novel and efficient carrier for pDNA with high dissociation efficiency.



中文翻译:

通过基本亮氨酸拉链结构域构建用于植物基因转染的肽/质粒 DNA 复合物

植物遗传修饰的一个重要方法是使用肽/pDNA复合物将基因转移到植物细胞中。对于传统的载体肽,肽序列必须含有大量的阳离子氨基酸以缩合和引入pDNA。因此,pDNA 从复合物中解离的效率很低,常常会引起问题。在此,我们设计了一种新的肽载体,模拟DNA结合蛋白的基本亮氨酸拉链(bZIP)结构域,其中(LU)4是亮氨酸拉链基序,(KUA)3是基本的DNA结合和细胞穿透结构域。基序(U = α-氨基异丁酸)。(KUA) 3 -(LU) 4肽与pDNA混合后,DNA分子凝聚形成约130 nm的纳米颗粒。此外,当将(KUA) 3 -(LU) 4肽和pDNA的复合物引入拟南芥( A. thaliana )的叶子时,在植物细胞中检测到报告蛋白的表达。因此,模拟bZIP结构域的(KUA) 3 -(LU) 4肽是一种新型且有效的pDNA载体,具有高解离效率。

更新日期:2024-03-05
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