Mayer John P, Zhang Faming, DiMarchi Richard D
Lilly Research Laboratories, Lilly Corporate Center, Indianapolis, IN 46285, USA.
Biopolymers. 2007;88(5):687-713. doi: 10.1002/bip.20734.
Throughout much of the last century insulin served a central role in the advancement of peptide chemistry, pharmacology, cell signaling and structural biology. These discoveries have provided a steadily improved quantity and quality of life for those afflicted with diabetes. The collective work serves as a foundation for the development of insulin analogs and mimetics capable of providing more tailored therapy. Advancements in patient care have been paced by breakthroughs in core technologies, such as semisynthesis, high performance chromatography, rDNA-biosynthesis and formulation sciences. How the structural and conformational dynamics of this endocrine hormone elicit its biological response remains a vigorous area of study. Numerous insulin analogs have served to coordinate structural biology and biochemical signaling to provide a first level understanding of insulin action. The introduction of broad chemical diversity to the study of insulin has been limited by the inefficiency in total chemical synthesis, and the inherent limitations in rDNA-biosynthesis and semisynthetic approaches. The goals of continued investigation remain the delivery of insulin therapy where glycemic control is more precise and hypoglycemic liability is minimized. Additional objectives for medicinal chemists are the identification of superagonists and insulins more suitable for non-injectable delivery. The historical advancements in the synthesis of insulin analogs by multiple methods is reviewed with the specific structural elements of critical importance being highlighted. The functional refinement of this hormone as directed to improved patient care with insulin analogs of more precise pharmacology is reported.
在上个世纪的大部分时间里,胰岛素在肽化学、药理学、细胞信号传导和结构生物学的发展中发挥了核心作用。这些发现为糖尿病患者的生活质量和数量提供了稳步改善。这些共同的工作为开发能够提供更个性化治疗的胰岛素类似物和模拟物奠定了基础。患者护理的进步得益于核心技术的突破,如半合成、高效色谱、重组DNA生物合成和制剂科学。这种内分泌激素的结构和构象动力学如何引发其生物学反应仍然是一个活跃的研究领域。许多胰岛素类似物有助于协调结构生物学和生化信号传导,以提供对胰岛素作用的初步理解。将广泛的化学多样性引入胰岛素研究受到全化学合成效率低下以及重组DNA生物合成和半合成方法固有局限性的限制。持续研究的目标仍然是提供血糖控制更精确、低血糖风险最小化的胰岛素治疗。药物化学家的其他目标是鉴定超级激动剂和更适合非注射给药的胰岛素。本文回顾了通过多种方法合成胰岛素类似物的历史进展,并强调了至关重要的特定结构元素。报道了这种激素的功能优化,旨在通过药理学更精确的胰岛素类似物改善患者护理。