Department of Chemical Biology, Max-Planck-Institute of Molecular Physiology, Otto-Hahn-Strasse 11, 44227, Dortmund, Germany.
Technische Universität Dortmund, Fakultät für Chemie und Chemische Biologie, Otto-Hahn-Strasse 6, 44227, Dortmund, Germany.
Chembiochem. 2019 Dec 13;20(24):2987-2990. doi: 10.1002/cbic.201900615. Epub 2019 Nov 19.
The acyl-binding UNC119 proteins mediate the activation and transport of various N-myristoylated proteins. In particular, UNC119a plays a crucial role in the completion of cytokinesis. Herein, we report the use of a lipidated peptide originating from the UNC119 binding partner Gnat1 as the basis for the design of lipidated, stabilized α-helical peptides that target UNC119a. By using the hydrocarbon peptide-stapling approach, cell-permeable binders of UNC119a were generated that induced the accumulation of cytokinetic and binucleated cells; this suggests UNC119a as a potential target for the inhibition of cytokinesis.
酰基结合 UNC119 蛋白介导各种 N-豆蔻酰化蛋白的激活和转运。特别是 UNC119a 在胞质分裂的完成中起着至关重要的作用。在此,我们报告了使用源自 UNC119 结合伴侣 Gnat1 的脂化肽作为设计靶向 UNC119a 的脂化、稳定化α-螺旋肽的基础。通过使用烃肽订书钉方法,生成了 UNC119a 的细胞穿透结合物,其诱导细胞分裂和双核细胞的积累;这表明 UNC119a 可能是抑制细胞分裂的潜在靶标。