Kircher Moritz F, Weissleder Ralph, Josephson Lee
Center for Molecular Imaging Research, Massachusetts General Hospital and Harvard Medical School, Charlestown, Massachusetts 02129, USA.
Bioconjug Chem. 2004 Mar-Apr;15(2):242-8. doi: 10.1021/bc034151d.
Near-infrared fluorescence (NIRF) optical probes have been able to provide a noninvasive assessment of enzyme activity for a number of different enzymes and types of pathology. Here we describe a dual fluorochrome enzyme-activatable probe featuring one NIRF fluorochrome that is activated by protease activity and a second fluorochrome that is protease resistant and serves as an internal standard. The probe was prepared by attaching Cy7 directly to an amino-CLIO, an amine functional cross-linked iron oxide (CLIO) nanoparticle carrier, in a protease resistant manner. Cy5.5 was attached to a protease sensitive polyarginine peptide spacer, also attached to amino-CLIO. In vitro and in vivo the ratio of the Cy5.5 to Cy7 fluorescence was increased by protease, reflecting the increase in Cy5.5 fluorescence by protease in the vicinity of the probe. In vitro and in vivo the absolute values of the Cy5.5 and Cy7 fluorescence reflected lesion size and the distance of lesions from the surface, while the ratio of Cy5.5 to Cy7 fluorescence obtained was constant and independent of lesion size and depth. The dual fluorochrome probe, and related dual wavelength imaging method, represents a novel approach for imaging protease activity in vivo.
近红外荧光(NIRF)光学探针已能够对多种不同的酶和病理类型进行酶活性的无创评估。在此,我们描述了一种双荧光团酶可激活探针,其具有一种由蛋白酶活性激活的近红外荧光团和第二种对蛋白酶具有抗性并用作内标的荧光团。该探针是通过将Cy7以抗蛋白酶的方式直接连接到氨基化超顺磁性氧化铁(CLIO)——一种胺功能化交联氧化铁(CLIO)纳米颗粒载体上制备而成的。Cy5.5连接到一个对蛋白酶敏感的聚精氨酸肽间隔臂上,该间隔臂也连接到氨基化CLIO上。在体外和体内,蛋白酶会使Cy5.5与Cy7荧光的比率增加,这反映了探针附近蛋白酶使Cy5.5荧光增强。在体外和体内,Cy5.5和Cy7荧光的绝对值反映了病变大小以及病变与表面的距离,而所获得的Cy5.5与Cy7荧光的比率是恒定的,且与病变大小和深度无关。这种双荧光团探针及相关的双波长成像方法代表了一种在体内对蛋白酶活性进行成像的新方法。