Department of Chemistry, Michigan State University, East Lansing, MI, 48824, USA.
Institute for Quantitative Health Sciences and Engineering, Michigan State University, East Lansing, MI, 48824, USA.
Sci Rep. 2020 Oct 15;10(1):17493. doi: 10.1038/s41598-020-74527-6.
People with type 1 diabetes (T1D) require exogenous administration of insulin, which stimulates the translocation of the GLUT4 glucose transporter to cell membranes. However, most bloodstream cells contain GLUT1 and are not directly affected by insulin. Here, we report that C-peptide, the 31-amino acid peptide secreted in equal amounts with insulin in vivo, is part of a 3-component complex that affects red blood cell (RBC) membranes. Multiple techniques were used to demonstrate saturable and specific C-peptide binding to RBCs when delivered as part of a complex with albumin. Importantly, when the complex also included Zn, a significant increase in cell membrane GLUT1 was measured, thus providing a cellular effect similar to insulin, but on a transporter on which insulin has no effect.
1 型糖尿病(T1D)患者需要外源性给予胰岛素,以刺激葡萄糖转运蛋白 4(GLUT4)向细胞膜移位。然而,大多数血液细胞含有 GLUT1,并且不受胰岛素的直接影响。在这里,我们报告说,C 肽是体内与胰岛素等量分泌的 31 个氨基酸肽,是影响红细胞(RBC)膜的 3 组分复合物的一部分。当作为与白蛋白的复合物的一部分递用时,使用多种技术证明了 C 肽与 RBC 的可饱和和特异性结合。重要的是,当复合物还包含 Zn 时,测量到细胞膜 GLUT1 显著增加,从而提供了类似于胰岛素的细胞作用,但作用于胰岛素没有作用的转运蛋白上。