Nishimura K, Frederick J, Kwatra M M
Department of Anesthesiology, Duke University Medical Center, Durham, NC 27710, USA.
J Recept Signal Transduct Res. 1998 Jan;18(1):51-65. doi: 10.3109/10799899809039164.
To identify the G proteins involved in the function of human substance P receptor (hSPR), the receptor was expressed in Sf9 cells using the baculovirus expression system. Maximal hSPR expression was up to 65 pmol/mg membrane protein. The following data indicated that hSPR in Sf9 membranes is coupled to endogenous G proteins: 1) binding of agonist radioligand [125I]BHSP to the receptor was sensitive to guanine nucleotides; and 2) stimulation of the receptor increased [35S]GTPgammaS binding. The hSPR-associated G proteins were identified by photoaffinity labeling with [alpha-32P]-azidoanilido GTP ([alpha-32P]AAGTP), followed by immunoprecipitation of the labeled G proteins with antibodies specific for various Galpha-subunits. These experiments showed that stimulation of hSPR in Sf9 membranes activated multiple endogenous G proteins including Galpha(o), Galpha(q/11), and Galpha(s). While hSPR's ability to associate with Gq/11 is well-documented, the present study provides the first evidence of hSPR's potential to activate Galpha(o) and Galpha(s).
为了鉴定参与人类P物质受体(hSPR)功能的G蛋白,利用杆状病毒表达系统在Sf9细胞中表达该受体。hSPR的最大表达量高达65 pmol/mg膜蛋白。以下数据表明Sf9膜中的hSPR与内源性G蛋白偶联:1)激动剂放射性配体[125I]BHSP与受体的结合对鸟嘌呤核苷酸敏感;2)受体的刺激增加了[35S]GTPγS的结合。通过用[α-32P]-叠氮苯胺基GTP([α-32P]AAGTP)进行光亲和标记,然后用针对各种Gα亚基的特异性抗体免疫沉淀标记的G蛋白,来鉴定与hSPR相关的G蛋白。这些实验表明,刺激Sf9膜中的hSPR可激活多种内源性G蛋白,包括Gα(o)、Gα(q/11)和Gα(s)。虽然hSPR与Gq/11结合的能力已有充分记录,但本研究首次提供了hSPR激活Gα(o)和Gα(s)潜力的证据。