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肽自组装成球形纳米颗粒,将亲水性部分递送至细胞质。

Self-assembly of peptides into spherical nanoparticles for delivery of hydrophilic moieties to the cytosol.

机构信息

Department of Clinical Sciences, King's College London School of Medicine, James Black Centre, 125 Coldharbour Lane, London, England.

出版信息

ACS Nano. 2010 May 25;4(5):2856-64. doi: 10.1021/nn901414q.

Abstract

We report a novel class of self-assembling peptide nanoparticles formed by mixing aqueous solutions of K(16) peptide and a 20 amino acid peptide of net charge -5 (GLFEALLELLESLWELLLEA). Particle formation is salt-dependent and yields perfectly spherical nanoparticles of approximately 120 to approximately 800 nm diameter, depending on buffer composition and temperature, with a stoichiometry of approximately 1:2.5 for the cationic and anionic peptides. The anionic peptide forms an alpha-helix in aqueous solution, has all five glutamates on one side of the helix, and exists entirely as a discrete oligomer of 9-10 peptides. A rigid oligomer with 45-50 negative charges almost certainly represents the core component of these nanoparticles, held together by electrostatic interactions with the unstructured K(16) peptide. Cells internalize these particles by an endocytic process, and free particles are frequently seen in the cytosol, presumably because of the acid-dependent fusogenic properties of the anionic peptide. Among other applications, these particles have potential for the targeted delivery of single or multiple therapeutic moieties directly to the cytosol, and we report the successful delivery of a K(16)-linked pro-apoptosis peptide.

摘要

我们报告了一类新型的自组装肽纳米颗粒,它们是由混合 K(16) 肽和带净电荷-5 的 20 个氨基酸肽水溶液形成的(GLFEALLELLESLWELLLEA)。颗粒的形成依赖于盐,并且根据缓冲液的组成和温度,生成直径约为 120 至 800nm 的完美球形纳米颗粒,阳离子和阴离子肽的比例约为 1:2.5。阴离子肽在水溶液中形成α-螺旋,其五个谷氨酸全部位于螺旋的一侧,并且完全以离散的 9-10 个肽的寡聚物存在。具有 45-50 个负电荷的刚性寡聚物几乎肯定代表了这些纳米颗粒的核心成分,通过与无规构象的 K(16) 肽的静电相互作用结合在一起。细胞通过内吞过程内化这些颗粒,并且细胞质中经常可以看到游离颗粒,这可能是由于阴离子肽的酸依赖性融合特性。在其他应用中,这些颗粒具有将单一或多种治疗部分直接靶向细胞质的靶向递送的潜力,我们报告了成功递送与 K(16) 连接的促凋亡肽。

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