Department of Molecular and Cellular Biology, Kennesaw State University, Kennesaw, Georgia.
Center for Tropical and Emerging Global Diseases, University of Georgia, Athens, Georgia.
Sci Rep. 2022 Nov 3;12(1):18572. doi: 10.1038/s41598-022-22054-x.
Trypanosoma brucei causes human African trypanosomiasis (HAT) and nagana in cattle. During infection of a vertebrate, endocytosis of host transferrin (Tf) is important for viability of the parasite. The majority of proteins involved in trypanosome endocytosis of Tf are unknown. Here we identify pseudokinase NRP1 (Tb427tmp.160.4770) as a regulator of Tf endocytosis. Genetic knockdown of NRP1 inhibited endocytosis of Tf without blocking uptake of bovine serum albumin. Binding of Tf to the flagellar pocket was not affected by knockdown of NRP1. However the quantity of Tf per endosome dropped significantly, consistent with NRP1 promoting robust capture and/or retention of Tf in vesicles. NRP1 is involved in motility of Tf-laden vesicles since distances between endosomes and the kinetoplast were reduced after knockdown of the gene. In search of possible mediators of NRP1 modulation of Tf endocytosis, the gene was knocked down and the phosphoproteome analyzed. Phosphorylation of protein kinases forkhead, NEK6, and MAPK10 was altered, in addition to EpsinR, synaptobrevin and other vesicle-associated proteins predicted to be involved in endocytosis. These candidate proteins may link NRP1 functionally either to protein kinases or to vesicle-associated proteins.
布氏锥虫引起人类非洲锥虫病(HAT)和牛的那加那病。在脊椎动物感染期间,内吞宿主转铁蛋白(Tf)对于寄生虫的存活至关重要。涉及锥虫内吞 Tf 的大多数蛋白质尚不清楚。在这里,我们将假激酶 NRP1(Tb427tmp.160.4770)鉴定为 Tf 内吞作用的调节剂。NRP1 的基因敲低抑制了 Tf 的内吞作用,而不会阻止牛血清白蛋白的摄取。NRP1 的基因敲低并不影响 Tf 与鞭毛窝的结合。然而,每个内体中的 Tf 量明显下降,这与 NRP1 促进 Tf 在囊泡中被强烈捕获和/或保留一致。NRP1 参与含 Tf 的囊泡的运动,因为基因敲低后内体与动基体之间的距离减少。为了寻找 NRP1 调节 Tf 内吞作用的可能介质,敲低了该基因并分析了磷酸化蛋白质组。除了 EpsinR、突触融合蛋白和其他预测参与内吞作用的囊泡相关蛋白外,叉头、NEK6 和 MAPK10 蛋白激酶的磷酸化也发生了改变。这些候选蛋白可能将 NRP1 功能上与蛋白激酶或囊泡相关蛋白联系起来。