Leibniz-Forschungsinstitut für Molekulare Pharmakologie (FMP), Berlin, Germany.
Institute of Chemistry and Biochemistry, Freie Universität Berlin, Berlin, Germany.
Nat Chem. 2021 Jun;13(6):530-539. doi: 10.1038/s41557-021-00661-x. Epub 2021 Apr 15.
Enabling the cellular delivery and cytosolic bioavailability of functional proteins constitutes a major challenge for the life sciences. Here we demonstrate that thiol-reactive arginine-rich peptide additives can enhance the cellular uptake of protein-CPP conjugates in a non-endocytic mode, even at low micromolar concentration. We show that such thiol- or HaloTag-reactive additives can result in covalently anchored CPPs on the cell surface, which are highly effective at co-delivering protein cargoes. Taking advantage of the thiol reactivity of our most effective CPP additive, we show that Cys-containing proteins can be readily delivered into the cytosol by simple co-addition of a slight excess of this CPP. Furthermore, we demonstrate the application of our 'CPP-additive technique' in the delivery of functional enzymes, nanobodies and full-length immunoglobulin-G antibodies. This new cellular uptake protocol greatly simplifies both the accessibility and efficiency of protein and antibody delivery, with minimal chemical or genetic engineering.
使功能性蛋白质能够在细胞内传递和在细胞质中具有生物利用度,这是生命科学面临的主要挑战。在这里,我们证明了巯基反应性精氨酸丰富肽添加剂可以增强蛋白-CPP 缀合物的细胞摄取,即使在低微摩尔浓度下也是如此。我们表明,这种巯基或 HaloTag 反应性添加剂可以在细胞表面上产生共价锚定的 CPP,这对于共同递送蛋白质货物非常有效。利用我们最有效的 CPP 添加剂的巯基反应性,我们表明,通过简单地共添加少量这种 CPP,含有半胱氨酸的蛋白质可以很容易地递送到细胞质中。此外,我们展示了我们的“CPP-添加剂技术”在功能性酶、纳米抗体和全长免疫球蛋白-G 抗体的递送上的应用。这种新的细胞摄取方案极大地简化了蛋白质和抗体递送的可及性和效率,而无需进行化学或遗传工程改造。