Uchida S, Matsumoto K, Takeyasu K, Higuchi H, Yoshida H
Life Sci. 1982 Jul 19;31(3):201-9. doi: 10.1016/0024-3205(82)90579-3.
The molecular sizes of the units concerned in 3-quinuclidinyl benzilate (QNB) binding and in the effects of guanine nucleotide and sulfhydryl reagent on the inhibition of QNB binding by carbachol in smooth muscle of guinea pig ileum were determined to be 76,000, 179,000 and 107,000, respectively by the radiation inactivation method. One or more subunits (GTP subunit) other than the receptor subunit in a muscarinic receptor appeared to be involved in the effect of guanine nucleotide. When guanine nucleotide was present, the receptor subunit seemed to be dissociated from the GTP subunit.
采用辐射失活法测定了有关3-喹核醇苯甲酸酯(QNB)结合以及鸟嘌呤核苷酸和巯基试剂对豚鼠回肠平滑肌中卡巴胆碱抑制QNB结合作用的分子大小,结果分别为76,000、179,000和107,000。毒蕈碱受体中除受体亚基外的一个或多个亚基(GTP亚基)似乎参与了鸟嘌呤核苷酸的作用。当存在鸟嘌呤核苷酸时,受体亚基似乎与GTP亚基解离。