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Delineation of the motilin domain involved in desensitization and internalization of the motilin receptor by using full and partial antagonists.

机译:通过使用完全和部分拮抗剂描述与胃动素受体的脱敏和内在化有关的胃动素结构域。

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Studies with fragments of the gastrointestinal peptide, motilin, indicate that the C-terminal region of this peptide plays an important role in the desensitization of the motilin receptor (MTLR). AIM: To verify this hypothesis we studied the desensitization, phosphorylation and internalization induced by motilin analogues of different chain length with agonistic and antagonistic properties in CHO-MTLR cells. METHODS: We studied motilin [1-22], the [1-14] fragment, the analogues Phe(3)[1-22] and Phe(3)[1-14], and two putative antagonists, GM-109 and MA-2029 (modified 1-4 and 1-3 fragments). Activation and desensitization (2h preincubation with the motilin analogues 10muM) were studied in CHO-MTLR cells by an aequorin based luminescence assay. Phosphorylation was studied by immunoprecipitation and internalization was visualized in CHO-MTLR cells containing an enhanced green fluorescent protein (CHO-MTLR-EGFP). RESULTS: Motilin [1-22] and [1-14] were more potent than Phe(3)[1-22] and Phe(3)[1-14] (pEC(50): 9.77, 8.78, 7.36 and 6.65, respectively) to induce Ca(2+) release. GM-109 and MA-2029 were without agonist activity. [1-22] and Phe(3)[1-22] decreased the second response to motilin from 78+/-2% to 11+/-3% and 34+/-3% (P<0.001), respectively, whereas [1-14], Phe(3)[1-14], GM-109 and MA-2029 had no desensitizing effect (68+/-5%, 78+/-3%, 78+/-6% and 78+/-5%, respectively, P>0.05). The rank order of MTLR-phosphorylation was: [1-22]>[1-14]>Phe(3)[1-22]=Phe(3)[1-14]>GM-109=MA-2029. Only motilin [1-22] and [1-14] induced receptor MTLR-EGFP internalization as shown by a decrease in membrane fluorescence: 20+/-3% and 7+/-3%, respectively. CONCLUSION: The C-terminus of motilin enhances desensitization, phosphorylation and internalization of the MTLR while modifications of the N-terminus can favor a conformation of the receptor that is less susceptible to phosphorylation and internalization.
机译:对胃肠道肽胃动素片段的研究表明,该肽的C端区域在胃动素受体(MTLR)的脱敏中起重要作用。目的:为验证这一假设,我们研究了不同链长的胃动素类似物在CHO-MTLR细胞中具有激动和拮抗特性的脱敏,磷酸化和内在化作用。方法:我们研究了胃动素[1-22],[1-14]片段,类似物Phe(3)[1-22]和Phe(3)[1-14],以及两种推定的拮抗剂GM-109和MA-2029(修饰的1-4和1-3片段)。通过基于水母发光蛋白的发光分析研究了CHO-MTLR细胞的激活和脱敏作用(与胃动素类似物10μM预孵育2h)。通过免疫沉淀研究了磷酸化作用,并在含有增强的绿色荧光蛋白(CHO-MTLR-EGFP)的CHO-MTLR细胞中观察到内在化。结果:胃动素[1-22]和[1-14]比Phe(3)[1-22]和Phe(3)[1-14]更有效(pEC(50):9.77、8.78、7.36和6.65 )分别诱导Ca(2+)释放。 GM-109和MA-2029没有激动剂活性。 [1-22]和Phe(3)[1-22]将对胃动素的第二反应分别从78 +/- 2%降低到11 +/- 3%和34 +/- 3%(P <0.001),而[1-14],Phe(3)[1-14],GM-109和MA-2029没有脱敏作用(68 +/- 5%,78 +/- 3%,78 +/- 6%和分别为78 +/- 5%,P> 0.05)。 MTLR-磷酸化的等级顺序为:[1-22]> [1-14]> Phe(3)[1-22] = Phe(3)[1-14]> GM-109 = MA-2029。如膜荧光降低所示,仅胃动素[1-22]和[1-14]诱导受体MTLR-EGFP内在化,分别为20 +/- 3%和7 +/- 3%。结论:胃动素的C末端增强了MTLR的脱敏,磷酸化和内在化,而N末端的修饰可以促进受体的构象,该构象不易被磷酸化和内在化。

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