Department of Chemistry, University of Pennsylvania, 231 South 34th Street, Philadelphia, PA, 19104-6323, USA.
Institute for Computational Molecular Science, College of Science and Technology, Temple University, 1925 N. 12th Street, Philadelphia, PA, 19122, USA.
Angew Chem Int Ed Engl. 2016 Jul 25;55(31):8984-7. doi: 10.1002/anie.201604055. Epub 2016 Jun 15.
Molecular imaging holds considerable promise for elucidating biological processes in normal physiology as well as disease states, but requires noninvasive methods for identifying analytes at sub-micromolar concentrations. Particularly useful are genetically encoded, single-protein reporters that harness the power of molecular biology to visualize specific molecular processes, but such reporters have been conspicuously lacking for in vivo magnetic resonance imaging (MRI). Herein, we report TEM-1 β-lactamase (bla) as a single-protein reporter for hyperpolarized (HP) (129) Xe NMR, with significant saturation contrast at 0.1 μm. Xenon chemical exchange saturation transfer (CEST) interactions with the primary allosteric site in bla give rise to a unique saturation peak at 255 ppm, well removed (≈60 ppm downfield) from the (129) Xe-H2 O peak. Useful saturation contrast was also observed for bla expressed in bacterial cells and mammalian cells.
分子成像是阐明正常生理和疾病状态下生物过程的有力手段,但需要非侵入性的方法来识别亚微米浓度的分析物。特别有用的是遗传编码的、单一蛋白质报告器,它利用分子生物学的力量来可视化特定的分子过程,但这种报告器在体内磁共振成像(MRI)中明显缺乏。在这里,我们报告 TEM-1 β-内酰胺酶(bla)作为超极化(HP)(129)Xe NMR 的单一蛋白质报告器,在 0.1μm 处具有显著的饱和对比度。与 bla 中的主要变构位点的氙气化学交换饱和转移(CEST)相互作用产生了一个独特的饱和峰,位于 255ppm,与(129)Xe-H2O 峰相差约 60ppm。在细菌细胞和哺乳动物细胞中表达的 bla 也观察到有用的饱和对比度。