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人Y1神经肽Y受体细胞外环中的酸性残基对于配体结合至关重要。

Acidic residues in extracellular loops of the human Y1 neuropeptide Y receptor are essential for ligand binding.

作者信息

Walker P, Munoz M, Martinez R, Peitsch M C

机构信息

Division of Hypertension, Centre Hospitalier Universitaire Vaudois, Lausanne, Switzerland.

出版信息

J Biol Chem. 1994 Jan 28;269(4):2863-9.

PMID:8300621
Abstract

To investigate whether negatively charged residues of the human Y1 neuropeptide Y (NPY) receptor are required for ligand binding, a series of mutants were constructed in which aspartic acid and glutamic acid residues present in putative extracellular domains of the Y1 receptor were systematically replaced by alanines. The mutant cDNAs were transiently expressed in HeLa cells using a vaccinia virus-derived expression system, and their ability to bind NPY was evaluated. The level of expression of mutants unable to bind NPY was also tested immunologically. In addition, the ability of the mutant proteins to be recruited to the cell surface was assessed by confocal microscopy. Substitution of aspartic acids and glutamic acids of the N-terminal first extracellular domain had no effect on binding. On the other hand, substitution of acidic residues present in the second, third, and fourth extracellular loops resulted in proteins unable to bind 125I-NPY. These results demonstrate that the extracellular loops of the human Y1 NPY receptor are essential portions of its ligand binding domain.

摘要

为了研究人Y1神经肽Y(NPY)受体的带负电荷残基是否为配体结合所必需,构建了一系列突变体,其中Y1受体假定细胞外结构域中存在的天冬氨酸和谷氨酸残基被丙氨酸系统取代。使用痘苗病毒衍生的表达系统在HeLa细胞中瞬时表达突变体cDNA,并评估它们结合NPY的能力。还通过免疫方法检测了无法结合NPY的突变体的表达水平。此外,通过共聚焦显微镜评估突变蛋白被募集到细胞表面的能力。N端第一个细胞外结构域的天冬氨酸和谷氨酸的取代对结合没有影响。另一方面,第二、第三和第四细胞外环中存在的酸性残基的取代导致蛋白质无法结合125I-NPY。这些结果表明,人Y1 NPY受体的细胞外环是其配体结合结构域的重要部分。

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