Department of Organic Chemistry, Institute for Molecules and Materials, Radboud University Nijmegen, The Netherlands.
J Control Release. 2010 Jul 1;145(1):33-9. doi: 10.1016/j.jconrel.2010.03.028. Epub 2010 Apr 8.
We report the design, synthesis, and characterization of a novel type of cationic lipopeptide, gemini-like amphiphilic peptides or 'geminoids'. As an example, the SPKR peptide, inspired by biological nucleic acid binding motifs, was appended with unsaturated (oleoyl/oleyl) alkyl tails. The compound shows remarkable DNA and siRNA delivery, without lysogenic helper lipid, in a variety of cells, with a moderate cytotoxic effect. It aggregates to nanoparticles that combine with DNA to lipoplexes, which undergo a change from lamellar to the more lysogenic hexagonal packing upon lowering the pH. The versatility of the chemical approach allowed us to study peptides related to SPKR, and to establish that the Pro and at least one of the cationic (Lys, Arg) residues are essential for the biological activity.
我们报告了一种新型阳离子脂肽的设计、合成和表征,即双亲和性肽或“脂肽类似物”。以 SPKR 肽为例,它受生物核酸结合基序的启发,被不饱和(油酰/油基)烷基尾修饰。该化合物在没有溶酶体辅助脂质的情况下,在多种细胞中表现出显著的 DNA 和 siRNA 传递作用,同时具有中等的细胞毒性。它聚集形成纳米颗粒,与 DNA 结合形成脂质体,当降低 pH 值时,脂质体从层状结构转变为更具溶酶体的六方堆积结构。这种化学方法的多功能性使我们能够研究与 SPKR 相关的肽,并确定 Pro 和至少一个阳离子(Lys、Arg)残基对生物活性是必需的。