Jeong Kwang Cheol, Yu Jae-Hyuk
Department of Animal Sciences and Emerging Pathogens Institute, University of Florida, Gainesville, FL, USA.
Methods Mol Biol. 2012;944:251-7. doi: 10.1007/978-1-62703-122-6_18.
Understanding in vivo protein-protein interactions is critical to dissect precise functions of the regulatory proteins of fungal secondary metabolites. As many fungi differentially produce a diverse array of secondary metabolites during their lifecycle, it is important to understand the cell-type specific regulation of secondary metabolism. However, due to the difficulty of sample preparation of biologically active proteins in fungal spores, protein-protein interaction studies have been generally restricted. While some outstanding studies revealed protein-protein interactions of selected regulators, including the velvet proteins in vegetative cells, a detailed protocol for investigating the protein-protein interactions in the fungal spores has not yet been reported. Here, we describe a working protocol for the purification and identification of interacting protein partners of the spores of Aspergillus nidulans employing the VelB protein as an example.
了解体内蛋白质-蛋白质相互作用对于剖析真菌次级代谢产物调控蛋白的精确功能至关重要。由于许多真菌在其生命周期中会差异地产生各种各样的次级代谢产物,因此了解次级代谢的细胞类型特异性调控非常重要。然而,由于在真菌孢子中制备生物活性蛋白质样品存在困难,蛋白质-蛋白质相互作用的研究通常受到限制。虽然一些出色的研究揭示了选定调节因子的蛋白质-蛋白质相互作用,包括营养细胞中的天鹅绒蛋白,但尚未报道用于研究真菌孢子中蛋白质-蛋白质相互作用的详细方案。在这里,我们以VelB蛋白为例,描述了一种用于纯化和鉴定构巢曲霉孢子相互作用蛋白伙伴的工作方案。