用于功能性蛋白质胞质递送的细胞表面保留肽添加剂

Cell-Surface-Retained Peptide Additives for the Cytosolic Delivery of Functional Proteins.

作者信息

Arafiles Jan Vincent V, Franke Jonathan, Franz Luise, Gómez-González Jacobo, Kemnitz-Hassanin Kristin, Hackenberger Christian P R

机构信息

Leibniz-Forschungsinstitut für Molekulare Pharmakologie (FMP), Robert-Rössle-Str. 10, Berlin 13125, Germany.

Institut für Chemie, Humboldt Universität zu Berlin, Brook-Taylor-Str. 2, Berlin 12489, Germany.

出版信息

J Am Chem Soc. 2023 Oct 31;145(45):24535-48. doi: 10.1021/jacs.3c05365.

Abstract

The delivery of functional proteins remains a major challenge in advancing biological and pharmaceutical sciences. Herein, we describe a powerful, simple, and highly effective strategy for the intracellular delivery of functional cargoes. Previously, we demonstrated that cell-penetrating peptide (CPP) additives equipped with electrophilic thiol-reactive moieties temporarily attach to the cellular membrane, thereby facilitating the cellular uptake of protein- and antibody-CPP cargoes through direct membrane transduction at low concentrations. Now, we hypothesize that CPP-additives with an increased retention on the cellular membrane will further enhance intracellular uptake. We discovered that adding a small hydrophobic peptide sequence to an arginine-rich electrophilic CPP-additive further improved the uptake of protein-CPP conjugates, whereas larger hydrophobic anchors showed increased cytotoxicity. Cell viability and membrane integrity measurements, structure-activity relationship studies, and quantitative evaluation of protein-CPP uptake revealed important design principles for cell-surface-retained CPP-additives. These investigations allowed us to identify a nontoxic, thiol-reactive CPP-additive containing the hydrophobic ILFF sequence, which can deliver fluorescent model proteins at low micromolar concentrations. This hydrophobic CPP-additive allowed the addition of protein cargoes for intracellular delivery after initial additive incubation. Time-lapse fluorescence microscopy and membrane tension analysis of cells treated with fluorescent ILFF-CPP-additives supported the claim of increased cell surface retention and suggested that the protein-CPP cargoes enter the cell through a mechanism involving lowered cell membrane tension. Finally, we demonstrated that our newly engineered hydrophobic CPP-additive enabled the uptake of a functional macrocyclic peptidic MDM2-inhibitor and a recombinant genome editing protein. This indicates that the developed hydrophobic CPP-additive holds promise as a tool to enhance the intracellular delivery of peptide and protein cargoes.

摘要

在推进生物科学和制药科学的过程中,功能性蛋白质的递送仍然是一项重大挑战。在此,我们描述了一种用于功能性货物细胞内递送的强大、简单且高效的策略。此前,我们证明,配备亲电硫醇反应性基团的细胞穿透肽(CPP)添加剂会暂时附着在细胞膜上,从而在低浓度下通过直接膜转导促进蛋白质和抗体 - CPP货物的细胞摄取。现在,我们假设在细胞膜上保留时间增加的CPP添加剂将进一步增强细胞内摄取。我们发现,向富含精氨酸的亲电CPP添加剂中添加一个小的疏水肽序列可进一步提高蛋白质 - CPP缀合物的摄取,而较大的疏水锚则显示出细胞毒性增加。细胞活力和膜完整性测量、构效关系研究以及蛋白质 - CPP摄取的定量评估揭示了细胞表面保留的CPP添加剂的重要设计原则。这些研究使我们能够鉴定出一种含有疏水ILFF序列的无毒、硫醇反应性CPP添加剂,它可以在低微摩尔浓度下递送荧光模型蛋白质。这种疏水CPP添加剂允许在初始添加剂孵育后添加用于细胞内递送的蛋白质货物。对用荧光ILFF - CPP添加剂处理的细胞进行的延时荧光显微镜观察和膜张力分析支持了细胞表面保留增加的说法,并表明蛋白质 - CPP货物通过一种涉及降低细胞膜张力的机制进入细胞。最后,我们证明我们新设计的疏水CPP添加剂能够摄取功能性大环肽MDM2抑制剂和重组基因组编辑蛋白质。这表明所开发的疏水CPP添加剂有望成为增强肽和蛋白质货物细胞内递送的工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7437/10655119/2bf11dee62cc/ja3c05365_0001.jpg

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