CNRS, IPBS (Institut de Pharmacologie et de Biologie Structurale), 205 Route de Narbonne, BP 64182, F-31077 Toulouse, France; Université de Toulouse, UPS, IPBS, F-31077 Toulouse, France.
INSERM UMR 1037, Cancer Research Center of Toulouse, 20-24 Rue du Pont St. Pierre, 31052 Toulouse Cedex, France; Université de Toulouse, 31052 Toulouse Cedex, France; Institut Claudius Regaud, 31052 Toulouse Cedex, France.
J Struct Biol. 2013 Sep;183(3):320-328. doi: 10.1016/j.jsb.2013.07.010. Epub 2013 Jul 31.
The need for early-on diagnostic tools to assess the folding and solubility of expressed protein constructs in vivo is of great interest when dealing with recalcitrant proteins. In this paper, we took advantage of the picomolar sensitivity of the bipartite GFP1-10/GFP11 system to investigate the solubility of the Mycobacterium tuberculosis 4'-phosphopantetheinyl transferase PptT, an enzyme essential for the viability of the tubercle bacillus. In vivo and in vitro complementation assays clearly showed the improved solubility of the full-length PptT compared to its N- and C-terminally truncated counterparts. However, initial attempts to purify the full-length enzyme overexpressed in Escherichia coli cells were hampered by aggregation issues overtime that caused the protein to precipitate within hours. The fact that the naturally occurring Coenzyme A and Mg(2+), essentials for PptT to carry out its function, could play a role in stabilizing the enzyme was confirmed using DSF experiments. In vitro activity assays were performed using the ACP substrate from the type I polyketide synthase PpsC from M. tuberculosis, a 2188 amino-acid enzyme that plays a major role in the virulence and pathogenicity of this microbial pathogen. We selected the most soluble and compact ACP fragment (2042-2188), identified by genetic selection of in-frame fragments from random library experiments, to monitor the transfer of the P-pant moiety from Coenzyme A onto a conserved serine residue of this ACP domain.
当涉及到棘手的蛋白质时,早期诊断工具对于评估体内表达的蛋白质结构的折叠和可溶性非常重要。在本文中,我们利用双组分 GFP1-10/GFP11 系统的皮摩尔灵敏度来研究结核分枝杆菌 4'-磷酸泛酰巯基乙胺转移酶 PptT 的可溶性,该酶是结核分枝杆菌生存所必需的酶。体内和体外互补测定清楚地表明,全长 PptT 的可溶性比其 N 和 C 端截断的对应物都得到了改善。然而,最初试图在大肠杆菌细胞中过表达全长酶时,由于聚集问题,该酶在数小时内沉淀,因此遇到了阻碍。使用 DSF 实验证实了自然存在的辅酶 A 和 Mg(2+)(PptT 发挥其功能所必需的)可能在稳定酶方面发挥作用。使用来自结核分枝杆菌 I 型聚酮合酶 PpsC 的 ACP 底物进行了体外活性测定,该酶是一种 2188 个氨基酸的酶,在这种微生物病原体的毒力和致病性中起主要作用。我们选择了最可溶和最紧凑的 ACP 片段(2042-2188),该片段是通过随机文库实验中的框内片段遗传选择来鉴定的,以监测 Coenzyme A 上的 P-pant 部分转移到该 ACP 结构域的保守丝氨酸残基上。