Russell H. Morgan Department of Radiology and Radiological Science, The Johns Hopkins University School of Medicine, Baltimore, Maryland 21287, USA.
J Am Chem Soc. 2013 Aug 21;135(33):12164-7. doi: 10.1021/ja403542g. Epub 2013 Aug 6.
Although metal ions are involved in a myriad of biological processes, noninvasive detection of free metal ions in deep tissue remains a formidable challenge. We present an approach for specific sensing of the presence of Ca(2+) in which the amplification strategy of chemical exchange saturation transfer (CEST) is combined with the broad range of chemical shifts found in (19)F NMR spectroscopy to obtain magnetic resonance images of Ca(2+). We exploited the chemical shift change (Δω) of (19)F upon binding of Ca(2+) to the 5,5'-difluoro derivative of 1,2-bis(o-aminophenoxy)ethane-N,N,N',N'-tetraacetic acid (5F-BAPTA) by radiofrequency labeling at the Ca(2+)-bound (19)F frequency and detection of the label transfer to the Ca(2+)-free (19)F frequency. Through the substrate binding kinetics we were able to amplify the signal of Ca(2+) onto free 5F-BAPTA and thus indirectly detect low Ca(2+) concentrations with high sensitivity.
尽管金属离子参与了无数的生物过程,但在深部组织中无创检测游离金属离子仍然是一个巨大的挑战。我们提出了一种方法,用于特异性检测 Ca(2+) 的存在,该方法将化学交换饱和转移 (CEST) 的放大策略与 (19)F NMR 光谱中发现的宽化学位移范围相结合,以获得 Ca(2+) 的磁共振图像。我们利用 Ca(2+)与 5,5'-二氟-1,2-双(邻氨基苯氧基)乙烷-N,N,N',N'-四乙酸的 5,5'-二氟衍生物(5F-BAPTA)结合时(19)F 的化学位移变化(Δω),通过在 Ca(2+)-结合(19)F 频率处进行射频标记,并检测标记转移到 Ca(2+)-游离(19)F 频率来实现。通过底物结合动力学,我们能够将 Ca(2+)的信号放大到游离的 5F-BAPTA 上,从而间接以高灵敏度检测低 Ca(2+)浓度。