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介质介导的分子内二硫键形成增强的巨胞饮诱导肽的发现。

Discovery of a Macropinocytosis-Inducing Peptide Potentiated by Medium-Mediated Intramolecular Disulfide Formation.

机构信息

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

Institute of Biomaterials and Bioengineering, Tokyo Medical and Dental University, 2-3-10 Kandasurugadai, Chiyoda-ku, Tokyo, 101-0062, Japan.

出版信息

Angew Chem Int Ed Engl. 2021 May 17;60(21):11928-11936. doi: 10.1002/anie.202016754. Epub 2021 Apr 14.

Abstract

Macropinocytosis is a ubiquitous cellular uptake mechanism of peptide-based intracellular delivery. This entry pathway shows promise as a route for the intracellular uptake of biomacromolecules and nanoparticles. In this work, we obtained the 8-residue analogue P4A bearing higher macropinocytosis induction ability. P4A contains vital cysteine residues in its sequence, which immediately reacts with cystine in culture medium to convert into its oxidized forms, including the intramolecularly oxidized form (oxP4A) as the dominant and active species. The conjugate of oxP4A and the membrane lytic peptide LK15 delivered bioactive proteins into cells; notably, this peptide delivered functional proteins fused with a negatively charged protein tag at a significantly reduced amount (up to nanomolar range) without compromising the delivery efficiency and the cellular activities of delivered proteins.

摘要

巨胞饮作用是一种普遍存在的细胞内肽类物质摄取机制,是生物大分子和纳米颗粒的细胞内摄取的有效途径。在这项工作中,我们获得了具有更高巨胞饮诱导能力的 8 残基类似物 P4A。P4A 序列中含有重要的半胱氨酸残基,它们会立即与培养基中的胱氨酸反应,转化为其氧化形式,包括以优势和活性形式存在的分子内氧化形式(oxP4A)。oxP4A 与溶膜肽 LK15 的缀合物将生物活性蛋白递送到细胞中;值得注意的是,这种肽以显著降低的量(低至纳摩尔范围)递送与带负电荷的蛋白质标签融合的功能性蛋白质,而不影响递送效率和递送到细胞中的蛋白质的细胞活性。

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