Goda Natsuko, Shimizu Kana, Kuwahara Yohta, Tenno Takeshi, Noguchi Tamotsu, Ikegami Takahisa, Ota Motonori, Hiroaki Hidekazu
Division of Structural Biology, Graduate School of Pharmaceutical Sciences, Nagoya University, Furo-cho, Chikusa-ku, Nagoya, Aichi 464-8601, Japan.
Computational Biology Research Center (CBRC), National Institute of Advanced Industrial Science and Technology (AIST), Tokyo Waterfront Bio-IT Research Building 2-4-7 Aomi, Koto-ku, Tokyo 135-0046, Japan.
Int J Mol Sci. 2015 Jul 10;16(7):15743-60. doi: 10.3390/ijms160715743.
Intrinsically disordered proteins (IDPs) that lack stable conformations and are highly flexible have attracted the attention of biologists. Therefore, the development of a systematic method to identify polypeptide regions that are unstructured in solution is important. We have designed an "indirect/reflected" detection system for evaluating the physicochemical properties of IDPs using nuclear magnetic resonance (NMR). This approach employs a "chimeric membrane protein"-based method using the thermostable membrane protein PH0471. This protein contains two domains, a transmembrane helical region and a C-terminal OB (oligonucleotide/oligosaccharide binding)-fold domain (named NfeDC domain), connected by a flexible linker. NMR signals of the OB-fold domain of detergent-solubilized PH0471 are observed because of the flexibility of the linker region. In this study, the linker region was substituted with target IDPs. Fifty-three candidates were selected using the prediction tool POODLE and 35 expression vectors were constructed. Subsequently, we obtained 15N-labeled chimeric PH0471 proteins with 25 IDPs as linkers. The NMR spectra allowed us to classify IDPs into three categories: flexible, moderately flexible, and inflexible. The inflexible IDPs contain membrane-associating or aggregation-prone sequences. This is the first attempt to use an indirect/reflected NMR method to evaluate IDPs and can verify the predictions derived from our computational tools.
缺乏稳定构象且高度灵活的内在无序蛋白(IDP)已引起生物学家的关注。因此,开发一种系统方法来识别溶液中无结构的多肽区域很重要。我们设计了一种“间接/反射”检测系统,用于使用核磁共振(NMR)评估IDP的物理化学性质。这种方法采用基于“嵌合膜蛋白”的方法,使用热稳定膜蛋白PH0471。该蛋白包含两个结构域,一个跨膜螺旋区域和一个C端OB(寡核苷酸/寡糖结合)折叠结构域(称为NfeDC结构域),由一个柔性接头连接。由于接头区域的灵活性,可以观察到去污剂溶解的PH0471的OB折叠结构域的NMR信号。在本研究中,接头区域被目标IDP取代。使用预测工具POODLE选择了53个候选物,并构建了35个表达载体。随后,我们获得了以25种IDP作为接头的15N标记的嵌合PH0471蛋白。NMR光谱使我们能够将IDP分为三类:灵活、中等灵活和不灵活。不灵活的IDP包含与膜相关或易于聚集的序列。这是首次尝试使用间接/反射NMR方法评估IDP,并可以验证从我们的计算工具得出的预测。