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甾醇化的巨胞饮诱导肽促进小细胞外囊泡的细胞摄取。

Stearylated Macropinocytosis-Inducing Peptides Facilitating the Cellular Uptake of Small Extracellular Vesicles.

机构信息

Institute for Chemical Research, Kyoto University, Uji, Kyoto 611-0011, Japan.

Graduate School of Science, Osaka Metropolitan University, Sakai, Osaka 599-8531, Japan.

出版信息

Bioconjug Chem. 2022 May 18;33(5):869-880. doi: 10.1021/acs.bioconjchem.2c00113. Epub 2022 May 4.

Abstract

Macropinocytosis is a form of endocytosis that allows massive uptake of extracellular materials and is a promising route for intracellular delivery of biofunctional macromolecules and nanoparticles. Our laboratory developed a potent macropinocytosis-inducing peptide named P4A. However, the ability of this peptide is not apparent in the presence of serum. This study aims to endow P4A and related peptides with the ability to induce macropinocytosis in the presence of serum by N-terminal acylation with long-chain fatty acids (i.e., decanoic, myristic, and stearic acids). Stearylated P4A (stearyl-P4A) had the highest effect on stimulating macropinocytotic uptake. Moreover, the intramolecularly disulfide-bridged analogue, stearyl-oxP4A, showed an even higher ability. The effect of stearyl-oxP4A to facilitate the intracellular delivery of small extracellular vesicles (sEVs) was evaluated in terms of (i) cellular uptake using sEVs labeled with an enhanced green fluorescent protein (EGFP) and (ii) cytosolic liberation and expression of sEV-encapsulated luciferase mRNA in recipient cells. The two- to threefold uptake of both sEVs in the presence of stearyl-oxP4A suggests the potential of the peptide for sEV delivery in the presence of serum.

摘要

巨胞饮作用是一种允许大量摄取细胞外物质的内吞作用形式,是将生物功能大分子和纳米颗粒递送到细胞内的有前途的途径。我们的实验室开发了一种名为 P4A 的有效巨胞饮作用诱导肽。然而,在血清存在的情况下,该肽的能力并不明显。本研究旨在通过 N 端酰化用长链脂肪酸(即癸酸、肉豆蔻酸和硬脂酸)赋予 P4A 及其相关肽在血清存在下诱导巨胞饮作用的能力。硬脂酰化 P4A(硬脂酰-P4A)对刺激巨胞饮摄取的效果最高。此外,分子内二硫键桥接类似物,硬脂酰-氧代 P4A(stearyl-oxP4A)显示出更高的能力。通过使用增强型绿色荧光蛋白(EGFP)标记的 sEV 评估硬脂酰-氧代 P4A 促进小细胞外囊泡(sEV)的细胞内递送的效果,(i)细胞摄取和(ii)在受者细胞中 sEV 包封的荧光素酶 mRNA 的细胞质释放和表达。在硬脂酰-氧代 P4A 的存在下,两种 sEV 的摄取增加了两到三倍,这表明该肽在血清存在下具有 sEV 递送的潜力。

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