Petrus Amanda K, Allis Damian G, Smith Robert P, Fairchild Timothy J, Doyle Robert P
Department of Chemistry, Syracuse University, Syracuse, NY 13244, USA.
ChemMedChem. 2009 Mar;4(3):421-6. doi: 10.1002/cmdc.200800346.
We recently reported a vitamin B(12) (B(12)) based insulin conjugate that produced significantly decreased blood glucose levels in diabetic STZ-rat models. The results of this study posed a fundamental question, namely what implications does B(12) conjugation have on insulin's interaction with the insulin receptor (IR)? To explore this question we used a combination of molecular dynamics simulations and immunoelectron microscopy, and the results are described herein. This investigation demonstrates that chemical modification of insulin by linking relatively large pendant groups does not inherently interfere with IR recognition. Furthermore, given that we have previously demonstrated a significant drop in blood glucose concentration following the oral administration of the B(12)-insulin bioconjugate used in this work, it is reasonable to conclude that the IR recognition described herein is associated with maintenance of biological activity for insulin. This outcome offers significant research scope for chemical modification of insulin with the purpose of improving oral-uptake efficiency.
我们最近报道了一种基于维生素B12(B12)的胰岛素缀合物,它在糖尿病链脲佐菌素诱导的大鼠模型中能显著降低血糖水平。这项研究的结果提出了一个基本问题,即B12缀合对胰岛素与胰岛素受体(IR)的相互作用有何影响?为了探究这个问题,我们结合了分子动力学模拟和免疫电子显微镜技术,结果在此处进行描述。这项研究表明,通过连接相对较大的侧链基团对胰岛素进行化学修饰并不会固有地干扰IR识别。此外,鉴于我们之前已经证明口服本文所用的B12-胰岛素生物缀合物后血糖浓度显著下降,有理由得出结论,本文所述的IR识别与胰岛素生物活性的维持有关。这一结果为通过化学修饰胰岛素来提高口服吸收效率提供了重要的研究空间。