Department of Biochemistry, University of Bayreuth, Bayreuth, Germany.
School of Chemistry, University of Bristol, Bristol, UK.
Nat Chem Biol. 2022 Sep;18(9):999-1004. doi: 10.1038/s41589-022-01076-6. Epub 2022 Jul 14.
Increasingly, it is possible to design peptide and protein assemblies de novo from first principles or computationally. This approach provides new routes to functional synthetic polypeptides, including designs to target and bind proteins of interest. Much of this work has been developed in vitro. Therefore, a challenge is to deliver de novo polypeptides efficiently to sites of action within cells. Here we describe the design, characterisation, intracellular delivery, and subcellular localisation of a de novo synthetic peptide system. This system comprises a dual-function basic peptide, programmed both for cell penetration and target binding, and a complementary acidic peptide that can be fused to proteins of interest and introduced into cells using synthetic DNA. The designs are characterised in vitro using biophysical methods and X-ray crystallography. The utility of the system for delivery into mammalian cells and subcellular targeting is demonstrated by marking organelles and actively engaging functional protein complexes.
越来越多的情况下,可以根据第一原理或通过计算设计从头开始的肽和蛋白质组装。这种方法为功能性合成多肽提供了新途径,包括针对和结合感兴趣的蛋白质的设计。这项工作的大部分是在体外进行的。因此,面临的一个挑战是将从头多肽有效地递送到细胞内的作用部位。在这里,我们描述了从头合成肽系统的设计、表征、细胞内递送和亚细胞定位。该系统由双重功能的碱性肽组成,既能穿透细胞又能与靶标结合,还有一个互补的酸性肽,可以与感兴趣的蛋白质融合,并使用合成 DNA 引入细胞。这些设计通过生物物理方法和 X 射线晶体学进行体外表征。该系统用于递送到哺乳动物细胞和亚细胞靶向的效用通过标记细胞器和主动参与功能蛋白复合物来证明。