Northeastern University, Center for Drug Discovery, 116 Mugar Life Sciences Building, Boston, Massachusetts 02115, USA.
J Proteome Res. 2010 Apr 5;9(4):1746-53. doi: 10.1021/pr900870p.
The human cannabinoid 1 receptor (hCB1), a ubiquitous G protein-coupled receptor (GPCR), transmits cannabinergic signals that participate in diverse (patho)physiological processes. Pharmacotherapeutic hCB1 targeting is considered a tractable approach for treating such prevalent diseases as obesity, mood disorders, and drug addiction. The hydrophobic nature of the transmembrane helices of hCB1 presents a formidable difficulty to its direct structural analysis. Comprehensive experimental characterization of functional hCB1 by mass spectrometry (MS) is essential to the targeting of affinity probes that can be used to define directly hCB1 binding domains using a ligand-assisted experimental approach. Such information would greatly facilitate the rational design of hCB1-selective agonists/antagonists with therapeutic potential. We report the first high-coverage MS analysis of the primary sequence of the functional hCB1 receptor, one of the few such comprehensive MS-based analyses of any GPCR. Recombinant C-terminal hexa-histidine-tagged hCB1 (His6-hCB1) was expressed in cultured insect (Spodoptera frugiperda) cells, solubilized by a procedure devised to enhance receptor purity following metal-affinity chromatography, desalted by buffer exchange, and digested in solution with (chymo)trypsin. "Bottom-up" nanoLC-MS/MS of the (chymo)tryptic digests afforded a degree of overall hCB1 coverage (>94%) thus far reported for only two other GPCRs. This MS-compatible procedure devised for His6-hCB1 sample preparation, incorporating in-solution (chymo)trypsin digestion in the presence of a low concentration of CYMAL-5 detergent, may be applicable to the MS-based proteomic characterization of other GPCRs. This work should help enable future ligand-assisted structural characterization of hCB1 binding motifs at the amino-acid level using rationally designed and targeted covalent cannabinergic probes.
人类大麻素 1 型受体(hCB1)是一种普遍存在的 G 蛋白偶联受体(GPCR),传递大麻素信号,参与多种(病理)生理过程。针对 hCB1 的药物治疗靶向被认为是治疗肥胖症、情绪障碍和药物成瘾等常见疾病的可行方法。hCB1 的跨膜螺旋的疏水性对其直接结构分析提出了巨大的挑战。通过质谱(MS)对功能性 hCB1 进行全面的实验表征对于靶向亲和探针至关重要,这些探针可以使用配体辅助实验方法直接定义 hCB1 结合域。这些信息将极大地促进具有治疗潜力的 hCB1 选择性激动剂/拮抗剂的合理设计。我们报告了第一个功能性 hCB1 受体(GPCR 中少数几个此类全面 MS 分析之一)的主要序列的高覆盖率 MS 分析。重组 C 末端六组氨酸标记的 hCB1(His6-hCB1)在培养的昆虫(草地贪夜蛾)细胞中表达,通过设计的方案进行溶解,该方案旨在增强金属亲和层析后受体的纯度,通过缓冲液交换进行脱盐,并在溶液中用(糜)蛋白酶进行消化。(糜)蛋白酶消化的“自上而下”nanoLC-MS/MS 提供了迄今为止仅报道的两种其他 GPCR 的总体 hCB1 覆盖率(>94%)。这种用于 His6-hCB1 样品制备的 MS 兼容程序,在存在低浓度 CYMAL-5 洗涤剂的情况下在溶液中进行(糜)蛋白酶消化,可能适用于其他 GPCR 的基于 MS 的蛋白质组学表征。这项工作应该有助于未来使用合理设计和靶向的共价大麻素探针,在氨基酸水平上辅助结构表征 hCB1 结合基序。