首页> 美国卫生研究院文献>Animal Cells and Systems >Luteinizing hormone-like and follicle-stimulating hormone-like activities of equine chorionic gonadotropin β-subunit mutants in cells expressing rat luteinizing hormone/chorionic gonadotropin receptor and rat follicle-stimulating hormone receptor
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Luteinizing hormone-like and follicle-stimulating hormone-like activities of equine chorionic gonadotropin β-subunit mutants in cells expressing rat luteinizing hormone/chorionic gonadotropin receptor and rat follicle-stimulating hormone receptor

机译:在表达大鼠叶丁骨激素/绒毛膜促性腺激素受体和大鼠卵泡刺激激素受体的细胞中大鼠绒毛膜促性腺激素β-亚基突变体的叶氏激素样和卵泡刺激的激素的活性。

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摘要

To identify the specific region of eCG involved in FSH-like activity, the following mutant expression vectors were constructed targeting the amino acid residues 102–104 of the eCG β-subunit: single mutants, eCGβV102G/α, eCGβF103P/α, and eCGβR104K/α; double mutants, eCGβV102G;F103P/α, eCGβV102G;R104K/α, and eCGβF103P;R104K/α; triple mutant, eCGβV102G;F103P;R104K/α. The LH-like and FSH-like activities of eCG mutants were examined in CHO-K1 cells expressing rat LH/CG receptor and rat FSH receptor. The levels of eCGβV102G/α, eCGβR104K/α, and eCGβV102G;R104K/α in the culture supernatant were markedly lower than those of eCGβ/α-wt. The other mutants and rec-eCGβ/α-wt were efficiently secreted into the culture supernatant. The LH-like activities of eCGV104G/α, eCGβV102G;R104K/α, and eCGβF103P;R104K/α were approximately 61%, 52%, and 54%, respectively, of those of eCG-wt. The Rmax values of the mutants were 58.9%–78.8% those of eCG-wt with eCGβR104K/α exhibiting the lowest value. The FSH-like activities of single mutants were only 16%–20% of those of eCG-wt. Additionally, the FSH-like activity of double mutants was less than 10% of that of eCG-wt. In particular, the FSH-like activities of βV102G;R104K/α and βF103P;R104K/α were 2.5–2.9% of that of eCG-wt. These results suggest that the amino acid residues 102–104 of the eCG β-subunit are dispensable and that the residue 104 of the eCG β-subunit plays a pivotal role in signal transduction through the rat FSH receptor. Thus, these mutants may aid future studies on eCG interactions with mammalian FSH receptors in vitro and in vivo.
机译:为了鉴定FSH样活动中涉及的ECG的特异性区域,构建了以下突变体表达载体的靶向ECGβ-亚基的氨基酸残基102-104:单突变体,ECGβV102G/α,ECGβF103P/α和ECGβR104K/ α;双突变体,ECGβV102G; F103P /α,ECGβV102G; R104K /α和ECGβF103P; R104K /α;三重突变体,ECGβV102G; F103P; R104K /α。在表达大鼠LH / CG受体和大鼠FSH受体的CHO-K1细胞中检查了ECG突变体的LH样和FSH样活动。 ECGβV102G/α,ECGβR104K/α和ECGβV102G的水平;培养上清液中的R104K /α显着低于ECGβ/α-WT的R104K /α。将其他突变体和REC-ECGβ/α-WT有效地分泌到培养上清液中。 ECGV104G /α,ECGβV102G; R104K /α和ECGβF103P的LH样活动; R104K /α分别为ECG-WT的61%,52%和54%。突变体的Rmax值为58.9%-78.8%,ECG-WT与ECGβR104K/α表现出最低值。单突变体的FSH样活动仅为ECG-WT的16%-20%。另外,双突变体的FSH样活性小于ECG-WT的10%。特别是,βv102g的fsh样活动; r104k /α和βf103p; r104k /α为ECG-wt的2.5-2.9%。这些结果表明ECGβ-亚基的氨基酸残基102-104可分配,并且ECGβ-亚基的残基104在通过大鼠FSH受体的信号转导中起着枢转作用。因此,这些突变体可以在体外和体内援助与哺乳动物FSH受体的ECG相互作用的未来研究。

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