基于分子和物理设计的葡萄糖响应型胰岛素。
Glucose-responsive insulin by molecular and physical design.
机构信息
Department of Chemical Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, USA.
Department of Biochemistry, Case Western Reserve University, Cleveland, Ohio 44106, USA.
出版信息
Nat Chem. 2017 Sep 22;9(10):937-943. doi: 10.1038/nchem.2857.
The concept of a glucose-responsive insulin (GRI) has been a recent objective of diabetes technology. The idea behind the GRI is to create a therapeutic that modulates its potency, concentration or dosing relative to a patient's dynamic glucose concentration, thereby approximating aspects of a normally functioning pancreas. From the perspective of the medicinal chemist, the GRI is also important as a generalized model of a potentially new generation of therapeutics that adjust potency in response to a critical therapeutic marker. The aim of this Perspective is to highlight emerging concepts, including mathematical modelling and the molecular engineering of insulin itself and its potency, towards a viable GRI. We briefly outline some of the most important recent progress toward this goal and also provide a forward-looking viewpoint, which asks if there are new approaches that could spur innovation in this area as well as to encourage synthetic chemists and chemical engineers to address the challenges and promises offered by this therapeutic approach.
葡萄糖响应型胰岛素(GRI)的概念是糖尿病技术的一个近期目标。GRI 的理念是创造一种治疗方法,使其效力、浓度或剂量相对于患者的动态血糖浓度进行调节,从而模拟正常胰腺的某些功能。从药物化学家的角度来看,GRI 也是一个重要的模型,代表了新一代潜在的治疗药物,它们可以根据关键治疗标志物来调整效力。本文的目的是强调一些新兴概念,包括数学建模和胰岛素本身及其效力的分子工程,以实现可行的 GRI。我们简要概述了实现这一目标的一些最重要的最新进展,并提供了前瞻性观点,即是否有新的方法可以激发该领域的创新,以及鼓励合成化学家与化学工程师应对这一治疗方法所带来的挑战和机遇。