Institute of Advanced Study, Kyushu University.
Proc Jpn Acad Ser B Phys Biol Sci. 2019;95(10):590-601. doi: 10.2183/pjab.95.040.
The need to measure the concentration of selected ions and small organic molecules in both in vivo and in vitro processes is continuously increasing beyond the borders of various research fields. This need has been fulfilled using "host-guest chemistry", or in general, by the use of "molecular recognition". The basic idea in these research fields was derived from the 1 : 1 host-guest interaction based on the "key-and-lock" concept. However, we have experienced that only with this classical concept, more precise, higher-order recognition faces serious difficulty. In this review article, I wish to explain that the introduction of two new concepts, i.e., the dynamic action of molecular systems and the amplification effect of molecular assemblies, overcame the limitation of the "key-and-lock" concept. In fact, we have found that even "complete" chirality segregation can be achieved under optimal conditions.
在各个研究领域的边界之外,不断有需要测量选定离子和小分子在体内和体外过程中的浓度的需求。这种需求已经通过“主体-客体化学”得到了满足,或者更普遍地说,通过“分子识别”得到了满足。这些研究领域的基本思想源自于基于“钥匙-锁”概念的 1:1 主体-客体相互作用。然而,我们已经体验到,仅凭借这个经典概念,更精确、更高阶的识别面临着严重的困难。在这篇综述文章中,我希望解释引入两个新概念,即分子系统的动态作用和分子组装的放大效应,克服了“钥匙-锁”概念的局限性。事实上,我们已经发现,即使在最佳条件下,也可以实现“完全”的手性分离。