Salthouse Christopher D, Reynolds Fred, Tam Jenny M, Josephson Lee, Mahmood Umar
Center for Molecular Imaging Research, Massachusetts General Hospital, Building 149, 13th Street, Room 5406, Charlestown, MA 02129-2060.
Sens Actuators B Chem. 2009 May 6;138(2):591-597. doi: 10.1016/j.snb.2009.02.037.
Proteases play important roles in a variety of pathologies from heart disease to cancer. Quantitative measurement of protease activity is possible using a novel spectrally matched dual fluorophore probe and a small animal lifetime imager. The recorded fluorescence from an activatable fluorophore, one that changes its fluorescent amplitude after biological target interaction, is also influenced by other factors including imaging probe delivery and optical tissue absorption of excitation and emission light.Fluorescence from a second spectrally matched constant (non-activatable) fluorophore on each nanoparticle platform can be used to correct for both probe delivery and tissue absorption. The fluorescence from each fluorophore is separated using fluorescence lifetime methods.
蛋白酶在从心脏病到癌症等多种病理过程中发挥着重要作用。使用新型光谱匹配双荧光团探针和小动物寿命成像仪可以对蛋白酶活性进行定量测量。可激活荧光团(即与生物靶点相互作用后荧光强度发生变化的荧光团)记录的荧光,也会受到其他因素的影响,包括成像探针递送以及激发光和发射光的光学组织吸收。每个纳米颗粒平台上第二个光谱匹配的恒定(不可激活)荧光团发出的荧光,可用于校正探针递送和组织吸收。使用荧光寿命方法分离每个荧光团发出的荧光。