在 Pichia pastoris 表达中使用 5-氟吲哚前体对 G 蛋白偶联受体 NK1R 中的色氨酸残基进行氟-19 标记。

IF 1.3 3区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY Journal of Biomolecular NMR Pub Date : 2024-03-30 DOI:10.1007/s10858-024-00439-6
Benxun Pan, Canyong Guo, Dongsheng Liu, Kurt Wüthrich
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引用次数: 0

摘要

在生物分子系统的核磁共振光谱分析中,使用氟-19 探针具有背景干净、灵敏度高等优点。因此,19F 标记程序受到广泛关注。在这里,我们使用 5-氟吲哚作为前体,将 5-氟色氨酸(5F-Trp)以低成本、高效率的特异残基方式引入到在 Pichia pastoris 中表达的 G 蛋白偶联受体(GPCR)中。该方法已在神经激肽 1 受体(NK1R)中成功应用。5F-Trp 标记的 NK1R 的 19F-NMR 光谱显示出一个分离良好的高场移共振,通过突变研究将其归属于 "切换开关色氨酸"。因此,通过残基选择性标记可以对这一重要功能残基进行特定位点研究。这里介绍的方法成本低廉,只需极少的遗传操作,可望适用于酵母表达整个 GPCR。
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Fluorine-19 labeling of the tryptophan residues in the G protein-coupled receptor NK1R using the 5-fluoroindole precursor in Pichia pastoris expression.

In NMR spectroscopy of biomolecular systems, the use of fluorine-19 probes benefits from a clean background and high sensitivity. Therefore, 19F-labeling procedures are of wide-spread interest. Here, we use 5-fluoroindole as a precursor for cost-effective residue-specific introduction of 5-fluorotryptophan (5F-Trp) into G protein-coupled receptors (GPCRs) expressed in Pichia pastoris. The method was successfully implemented with the neurokinin 1 receptor (NK1R). The 19F-NMR spectra of 5F-Trp-labeled NK1R showed one well-separated high field-shifted resonance, which was assigned by mutational studies to the "toggle switch tryptophan". Residue-selective labeling thus enables site-specific investigations of this functionally important residue. The method described here is inexpensive, requires minimal genetic manipulation and can be expected to be applicable for yeast expression of GPCRs at large.

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来源期刊
Journal of Biomolecular NMR
Journal of Biomolecular NMR 生物-光谱学
CiteScore
6.00
自引率
3.70%
发文量
19
审稿时长
6-12 weeks
期刊介绍: The Journal of Biomolecular NMR provides a forum for publishing research on technical developments and innovative applications of nuclear magnetic resonance spectroscopy for the study of structure and dynamic properties of biopolymers in solution, liquid crystals, solids and mixed environments, e.g., attached to membranes. This may include: Three-dimensional structure determination of biological macromolecules (polypeptides/proteins, DNA, RNA, oligosaccharides) by NMR. New NMR techniques for studies of biological macromolecules. Novel approaches to computer-aided automated analysis of multidimensional NMR spectra. Computational methods for the structural interpretation of NMR data, including structure refinement. Comparisons of structures determined by NMR with those obtained by other methods, e.g. by diffraction techniques with protein single crystals. New techniques of sample preparation for NMR experiments (biosynthetic and chemical methods for isotope labeling, preparation of nutrients for biosynthetic isotope labeling, etc.). An NMR characterization of the products must be included.
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