Brandenburg D, Diaconescu C, Saunders D, Thamm P
Nature. 1980 Aug 21;286(5775):821-2. doi: 10.1038/286821a0.
The first step of insulin's many cellular functions is specific binding to receptors on the plasma membrane of target cells. The subsequent molecular basis of insulin action, particularly the coupling mechanism(s) involved in transmitting the biological message, remains largely unknown. Our approach to the problem centres on the application of a series of well characterized photo-insulins carrying an aryl-azido or nitro-aryl-azido group in positions A1, B1, B2 or B29 (refs 2--4). Specific binding to membrane components could be demonstrated with B1-, B29- (ref. 5) and A1-photo-insulins as well as a B2-derivative. We now report that lipogenesis is increased to, and maintained at, near-maximal levels for several hours after photoinduced covalent binding of B2- (2-nitro,4-azidophenylacetyl)-des-PheB1-insulin (Napa-DP-insulin) to living adipocytes.
胰岛素众多细胞功能的第一步是与靶细胞质膜上的受体特异性结合。胰岛素作用的后续分子基础,尤其是参与传递生物信息的偶联机制,在很大程度上仍然未知。我们解决这个问题的方法集中在应用一系列在A1、B1、B2或B29位带有芳基叠氮或硝基芳基叠氮基团的特征明确的光胰岛素(参考文献2 - 4)。B1 -、B29 -(参考文献5)和A1 -光胰岛素以及一种B2衍生物能够证明与膜成分的特异性结合。我们现在报告,在光诱导的B2 -(2 -硝基,4 -叠氮基苯基乙酰基)-去苯丙氨酸B1 -胰岛素(Napa - DP -胰岛素)与活脂肪细胞共价结合后,脂肪生成增加并在数小时内维持在接近最大水平。