首页> 美国卫生研究院文献>Frontiers in Physiology >The N-terminal cytoplasmic region of NCBE displays features of an intrinsic disordered structure and represents a novel target for specific drug screening
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The N-terminal cytoplasmic region of NCBE displays features of an intrinsic disordered structure and represents a novel target for specific drug screening

机译:NCBE的N末端胞质区显示出固有的无序结构特征并代表了特异性药物筛选的新靶标

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摘要

The sodium dependent bicarbonate transporter NCBE/NBCn2 is predominantly expressed in the central nervous system (CNS). The highest protein concentrations are found in the choroid plexus. The primary function of this integral plasma membrane transport protein is to regulate intracellular neuronal pH and also probably to maintain the pH homeostasis across the blood-cerebrospinal fluid barrier. NCBE is predicted to contain at least 10 transmembrane helices. The N- and C- termini are both cytoplasmic, with a large N-terminal domain (Nt-NCBE) and a relatively small C-terminal domain (Ct-NCBE). The Nt-NCBE is likely to be involved in bicarbonate recognition and transport and contains key areas of regulation involving pH sensing and protein-protein interactions. Intrinsic disordered protein regions (IDPRs) are defined as protein regions having no rigid three-dimensional structure under physiological conditions. They are believed to be involved in signaling networks in which specific, low affinity, protein-protein interactions play an important role. We predict that NCBE and other SoLute Carrier 4 (SLC4) family members have a high level of intrinsic disorder in their cytoplasmic regions. To provide biophysical evidence for the IDPRs predicted in Nt-NCBE, we produced pure (>99%), recombinant Nt-NCBE using E. coli as the expression host. The protein was used to perform differential scanning fluorescence spectroscopy (DSF), in order to search for small molecules that would induce secondary or tertiary structure in the IDPRs. We expect this to assist the development of selective pharmaceutical compounds against individual SLC4 family members. We have also determined a low resolution (4 Å) X-ray crystal structure of the N-terminal core domain. The N-terminal cytoplasmic domain (cdb3) of anion exchanger 1 (AE1) shares a similar fold with the N-terminal core domain of NCBE. Crystallization conditions for the full-length N-terminal domain have been sought, but only the core domain yields diffracting crystals.
机译:钠依赖性碳酸氢盐转运蛋白NCBE / NBCn2主要在中枢神经系统(CNS)中表达。在脉络丛中发现最高的蛋白质浓度。这种完整的质膜转运蛋白的主要功能是调节细胞内神经元pH值,还可能维持跨血脑脊液屏障的pH稳态。预计NCBE至少包含10个跨膜螺旋。 N末端和C末端都是细胞质的,具有大的N末端结构域(Nt-NCBE)和相对小的C末端结构域(Ct-NCBE)。 Nt-NCBE可能参与碳酸氢盐的识别和转运,并且包含涉及pH传感和蛋白质-蛋白质相互作用的关键调控领域。固有无序蛋白区域(IDPR)被定义为在生理条件下不具有刚性三维结构的蛋白区域。据信它们参与信号传导网络,其中特异性,低亲和力的蛋白质-蛋白质相互作用起重要作用。我们预测NCBE和其他SoLute载体4(SLC4)家庭成员在其细胞质区域具有高水平的内在疾病。为了提供Nt-NCBE中预测的IDPR的生物物理证据,我们使用大肠杆菌作为表达宿主,生产了纯净的(> 99%)重组Nt-NCBE。为了寻找在IDPR中诱导二级或三级结构的小分子,使用了该蛋白质来进行差示扫描荧光光谱(DSF)。我们希望这有助于开发针对单个SLC4家族成员的选择性药物化合物。我们还确定了N端核心域的低分辨率(4Å)X射线晶体结构。阴离子交换剂1(AE1)的N末端胞质域(cdb3)与NCBE的N末端核心域共享相似的折叠。寻找全长N-末端结构域的结晶条件,但是仅核心结构域产生衍射晶体。

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