Matsumoto K, Uchida S, Takeyasu K, Higuchi H, Yoshida H
Life Sci. 1982 Jul 19;31(3):211-20. doi: 10.1016/0024-3205(82)90580-x.
Trypsin-treatment of the microsome fraction of the ileum and the synaptic membrane fraction of the cerebral cortex of guinea-pig caused selective reduction in the apparent affinity of an agonist (carbachol), but not an antagonist (atropine), to muscarinic acetylcholine receptors (mAChR), measured as inhibition of binding of 3H-quinuclidinyl benzilate (3H-QNB). This effect was similar to that of Gpp(NH)p. The effects of trypsin and Gpp(NH)p were not additive. On the other hand, treatment of these fractions with 5,5'-dithiobis (2-nitrobenzoic acid) (DTNB) increased the apparent affinity of agonist, but not antagonist. The effect of DTNB predominated over those of trypsin and Gpp(NH)p, when the fractions were treated with two reagents simultaneously.
用胰蛋白酶处理豚鼠回肠的微粒体部分和大脑皮层的突触膜部分,导致激动剂(卡巴胆碱)而非拮抗剂(阿托品)对毒蕈碱型乙酰胆碱受体(mAChR)的表观亲和力选择性降低,这通过抑制³H-喹核醇基苯甲酸酯(³H-QNB)的结合来测定。这种效应与Gpp(NH)p的效应相似。胰蛋白酶和Gpp(NH)p的效应并非相加。另一方面,用5,5'-二硫代双(2-硝基苯甲酸)(DTNB)处理这些部分会增加激动剂而非拮抗剂的表观亲和力。当这些部分同时用两种试剂处理时,DTNB的效应比胰蛋白酶和Gpp(NH)p的效应更显著。