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Modulation of Luminescence Intensity of Lanthanide Complexes by Photoinduced Electron Transfer and Its Application to a Long-Lived Protease Probe

机译:光诱导电子转移调控镧系元素配合物的发光强度及其在长寿蛋白酶探针中的应用

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摘要

Luminescent lanthanide complexes (Tb~(3+),Eu~(3+),etc.)have excellent properties for biological applications,including extraordinarily long lifetimes and large Stokes shifts.However,there have been few reports of lanthanide-based functional probes,because of the difficulty in designing suitable complexes with a luminescent on/off switch.Here,we have synthesized a series of complexes which consist of three moieties:a lanthanide chelate,an antenna,and a luminescence off/on switch.The antenna is an aromatic ring which absorbs light and transmits its energy to the metal,and the switch is a benzene derivative with a different HOMO level.If the HOMO level is higher than a certain threshold,the complex emits no luminescence at all,which indicates that the lanthanide luminescence can be modulated by photoinduced electron transfer (PeT)from the switch to the sensitizer.This approach to control lanthanide luminescence makes possible the rational design of functional lanthanide complexes,in which the luminescence property is altered by a biological reaction.To exemplify the utility of our approach to the design of lanthanide complexes with a switch,we have developed a novel protease probe,which undergoes a significant change in luminescence intensity upon enzymatic cleavage of the substrate peptide.This probe,combined with time-resolved measurements,was confirmed in model experiments to be useful for the screening of inhibitors,as well as for clinical diagnosis.
机译:发光镧系元素络合物(Tb〜(3 +),Eu〜(3+)等)在生物学应用中具有优异的性能,包括超长的寿命和较大的斯托克斯位移(Stokes shift),但是基于镧系元素的功能探针的报道很少。由于难以设计具有发光开/关开关的配合物。在这里,我们合成了一系列由三个部分组成的配合物:镧系元素螯合物,天线和发光关/开开关。吸收光并将其能量传递给金属的芳香环,而开关是具有不同HOMO能级的苯衍生物。如果HOMO能级高于某个阈值,则该络合物根本不会发光。镧系元素的发光可以通过从开关到敏化剂的光致电子转移(PeT)进行调节。这种控制镧系元素发光的方法使功能性镧系元素络合物的合理设计成为可能。为了证明我们的方法通过开关设计镧系元素配合物的效用,我们开发了一种新型的蛋白酶探针,该酶探针在被底物肽酶解后,其发光强度发生了显着变化。该探针与时间分辨测量相结合,已在模型实验中得到证实,可用于筛选抑制剂和用于临床诊断。

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  • 来源
    《Journal of the American Chemical Society》 |2006年第21期|p.6938-6946|共9页
  • 作者单位

    Contribution from the Graduate School of Pharmaceutical Sciences,The University of Tokyo,7-3-1 Hongo,Bunkyo-ku,Tokyo 113-0033,Japan,CREST,JST,4-1-8 Honcho,Kawaguchi,Saitama,332-0012,Japan,Department of Material and Life Science,Division of Advanced S;

    Contribution from the Graduate School of Pharmaceutical Sciences,The University of Tokyo,7-3-1 Hongo,Bunkyo-ku,Tokyo 113-0033,Japan,CREST,JST,4-1-8 Honcho,Kawaguchi,Saitama,332-0012,Japan,Department of Material and Life Science,Division of Advanced S;

    Contribution from the Graduate School of Pharmaceutical Sciences,The University of Tokyo,7-3-1 Hongo,Bunkyo-ku,Tokyo 113-0033,Japan,CREST,JST,4-1-8 Honcho,Kawaguchi,Saitama,332-0012,Japan,Department of Material and Life Science,Division of Advanced S;

    Contribution from the Graduate School of Pharmaceutical Sciences,The University of Tokyo,7-3-1 Hongo,Bunkyo-ku,Tokyo 113-0033,Japan,CREST,JST,4-1-8 Honcho,Kawaguchi,Saitama,332-0012,Japan,Department of Material and Life Science,Division of Advanced S;

    Contribution from the Graduate School of Pharmaceutical Sciences,The University of Tokyo,7-3-1 Hongo,Bunkyo-ku,Tokyo 113-0033,Japan,CREST,JST,4-1-8 Honcho,Kawaguchi,Saitama,332-0012,Japan,Department of Material and Life Science,Division of Advanced S;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 化学;
  • 关键词

  • 入库时间 2022-08-18 03:22:42

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