Rimele T J, Gaginella T S
Biochem Pharmacol. 1982 Feb 15;31(4):515-20. doi: 10.1016/0006-2952(82)90153-8.
The widely used muscarinic receptor ligand [3H]quinuclidinyl benzilate ([3H]QNB) was found to bind in a site-specific but artifactual manner to rat intestinal mucus, obscuring specific binding to muscarinic receptors on intestinal epithelial cells. Atropine inhibited [3H]QNB binding to mucus with an apparent IC50 of 2.1 x 10(-7) M, compared to an IC50 of 1.4 x 10(-8) M obtained with a homogenate of intestinal epithelial cells. Unlabeled QNB also inhibited binding of [3H]QNB to mucus but the apparent IC50 (4 x 10(-7) M) was about 300-fold greater than the IC50 determined with a control tissue, heart muscle (IC50, 1.2 x 10(-9) M). [3H]QNB binding was saturable over the concentration range of 1-7 nM in the heart, with an apparent KD of 0.76 nM. As expected from the high IC50 for QNB in the mucus binding experiments, binding to mucus was not saturable over the 1-15 nM concentration range. Based on pH profiles and temperature dependency of binding, it seems unlikely that mucin, the primary component of mucus, was responsible for [3H]QNB binding to the mucus. The findings have implications for studies which involve binding of [3H]QNB in particular and other ligands in general to mucus-secreting epithelial tissues.
人们发现,广泛使用的毒蕈碱受体配体[3H]喹核醇基苯甲酸酯([3H]QNB)以位点特异性但人为的方式与大鼠肠道黏液结合,从而掩盖了其与肠道上皮细胞上毒蕈碱受体的特异性结合。阿托品抑制[3H]QNB与黏液的结合,其表观IC50为2.1×10(-7)M,而肠道上皮细胞匀浆的IC50为1.4×10(-8)M。未标记的QNB也抑制[3H]QNB与黏液的结合,但表观IC50(4×10(-7)M)比用对照组织心肌测定的IC50(1.2×10(-9)M)大约高300倍。在心脏中,[3H]QNB结合在1-7 nM的浓度范围内是可饱和的,表观KD为0.76 nM。正如在黏液结合实验中QNB的高IC50所预期的那样,在1-15 nM浓度范围内,与黏液的结合是不饱和的。根据结合的pH曲线和温度依赖性,黏液的主要成分黏蛋白似乎不太可能是[3H]QNB与黏液结合的原因。这些发现对涉及[3H]QNB以及一般其他配体与分泌黏液的上皮组织结合的研究具有启示意义。