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通过免疫印迹法鉴定大鼠胰腺细胞系中的生长抑素前体形式。

Identification by immunoblotting of somatostatin proforms in a rat pancreatic cell line.

作者信息

Lherisson C, Svoboda M, Pradayrol L, Estival A, Christophe J, Vaysse N

机构信息

INSERM, U151 Toulouse, France.

出版信息

Pancreas. 1988;3(6):668-74. doi: 10.1097/00006676-198812000-00007.

Abstract

The immunoblotting technique is applied to the analysis of "somatostatin" compounds secreted by R.I.N. T3 cells. We can confirm that two proforms of 15,300 +/- 750 and 29,000 +/- 1,100 Da accumulate in the extracellular medium. The unexpected form of 29 kDa, probably a dimeric form, disappears in reducing conditions. However, the 15 kDa peptide is characterized by several antibodies directed against either the intramolecular cycle of somatostatin-14 or the N-terminal extension of somatostatin-28. The 15 kDa form presents the same electrophoretic mobility in SDS-PAGE than the prosomatostatin isolated from a hypothalamic extract. Furthermore, this compound corresponds to the calculated mass of 10,388 Da deduced from the cDNA sequence. The detection of an immunoreactive 6 kDa peptide in the gel filtration fractions suggests an intermediate step in the prosomatostatin processing in these cells.

摘要

免疫印迹技术应用于分析R.I.N. T3细胞分泌的“生长抑素”化合物。我们可以证实,两种前体形式,分子量分别为15,300 +/- 750道尔顿和29,000 +/- 1,100道尔顿,在细胞外培养基中积累。分子量为29 kDa的意外形式,可能是二聚体形式,在还原条件下消失。然而,15 kDa的肽段可被几种针对生长抑素-14分子内环或生长抑素-28 N端延伸的抗体识别。15 kDa形式在SDS-PAGE中的电泳迁移率与从下丘脑提取物中分离的前生长抑素相同。此外,该化合物的分子量与根据cDNA序列推导的计算质量10,388道尔顿相符。在凝胶过滤级分中检测到免疫反应性6 kDa肽段,表明这些细胞中前生长抑素加工过程存在中间步骤。

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