Musso G F, Assoian R K, Kaiser E T, Kézdy F J, Tager H S
Biochem Biophys Res Commun. 1984 Mar 15;119(2):713-9. doi: 10.1016/s0006-291x(84)80309-5.
A glucagon analog with the following sequence has been synthesized: His- Ser-Gln-Gly-Thr-Phe-Thr-Ser-Asp-Tyr-Ser-Lys-Tyr-Leu-Asp-Ser-Arg-Arg -Leu-Gln-Glu-Phe-Leu-Gln-Trp-Ala-Leu-Gln-Thr. When interacting with rat hepatocytes, the analog mimics, in part, the activities of glucagon in receptor binding and inhibition of carbohydrate incorporation into glycogen. Comparison of the binding of the analog with that of glucagon demonstrates the existence of two distinct homogeneous populations of glucagon receptors. The synthetic analog acts as a specific probe for those receptors that have a high affinity for glucagon.
组氨酸-丝氨酸-谷氨酰胺-甘氨酸-苏氨酸-苯丙氨酸-苏氨酸-丝氨酸-天冬氨酸-酪氨酸-丝氨酸-赖氨酸-酪氨酸-亮氨酸-天冬氨酸-丝氨酸-精氨酸-精氨酸-亮氨酸-谷氨酰胺-谷氨酸-苯丙氨酸-亮氨酸-谷氨酰胺-色氨酸-丙氨酸-亮氨酸-谷氨酰胺-苏氨酸。当与大鼠肝细胞相互作用时,该类似物部分模拟了胰高血糖素在受体结合以及抑制碳水化合物掺入糖原方面的活性。该类似物与胰高血糖素结合的比较表明存在两种不同的均一胰高血糖素受体群体。合成的类似物可作为对那些对胰高血糖素具有高亲和力的受体的特异性探针。