文章基本信息

标题：Fatty acylation enhances the cellular internalization and cytosolic distribution of a cystine-knot peptide
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作者：Xinxin Gao ; Ann De Mazière ; Rhiannon Beard 等
期刊名称：iScience
印刷版ISSN：2589-0042
出版年度：2021
卷号：24
期号：11
页码：1-18
DOI：10.1016/j.isci.2021.103220
语种：English
出版社：Elsevier
摘要：SummaryDelivering peptides into cells could open up possibilities for targeting intracellular proteins. Although fatty acylation of peptide therapeutics improves their systemic half-life, it remains unclear how it influences their cellular uptake. Here, we demonstrate that a fatty acylated peptide exhibits enhanced cellular internalization and cytosolic distribution compared to the un-acylated version. By using a cystine-knot peptide as a model system, we report an efficient strategy for site-specific conjugation of fatty acids. Peptides modified with fatty acids of different chain lengths entered cells through clathrin-mediated and macropinocytosis pathways. The cellular uptake was mediated by the length of the hydrocarbon chain, with myristic acid conjugates displaying the highest distribution across the cytoplasm including the cytosol, and endomembranes of the ER, Golgi and mitochondria. Our studies demonstrate how fatty acylation improves the cellular uptake of peptides, and lay the groundwork for future development of bioactive peptides with enhanced intracellular distribution.Graphical abstractDisplay OmittedHighlights•A synthetic strategy comprises site-specific conjugation of fatty acids to peptides•Fatty acylation of a peptide enhances its cellular uptake and cytosolic distribution•Myristoylated peptides display a high cytoplasmic distribution•Fatty acylated peptides are internalized via multiple endocytic routesBiological sciences; Biochemistry; Biochemical engineering; Biotechnology