Yoo Byunghee, Raam Manu S, Rosenblum Rachel M, Pagel Mark D
Case Center of Imaging Research and Department of Biomedical Engineering, Case Western Reserve University, Cleveland, OH 44106, USA.
Contrast Media Mol Imaging. 2007 Jul;2(4):189-98. doi: 10.1002/cmmi.145.
Proteases are important biomarkers for many biological processes and are popular targets for therapeutics investigations. A protease can be detected by monitoring changes in the paramagnetic chemical exchange saturation transfer (PARACEST) effect of a MRI contrast agent that serves as a substrate for the protease. To translate this type of responsive PARACEST MRI contrast agent to in vivo applications, the sensitivity, timing, specificity and validation of the response of the agent must be evaluated. This report demonstrates that PARACEST MRI contrast agents can be used to detect nanomolar concentrations of proteases, can be designed to preferentially detect the protease caspase-3 relative to caspase-8, and can be detected within the 15 min time frame of typical MRI studies. The response can be validated using an unresponsive PARACEST MRI contrast agent as a control. A survey of the MEROPS database shows that this approach may also be applied to detect other proteases, and therefore may represent a new platform technology for studies of the proteasome.
蛋白酶是许多生物过程的重要生物标志物,也是治疗学研究的热门靶点。蛋白酶可以通过监测作为蛋白酶底物的磁共振成像(MRI)造影剂的顺磁化学交换饱和转移(PARACEST)效应的变化来检测。为了将这种类型的响应性PARACEST MRI造影剂转化为体内应用,必须评估该造影剂响应的灵敏度、时间、特异性和验证。本报告表明,PARACEST MRI造影剂可用于检测纳摩尔浓度的蛋白酶,可设计为相对于半胱天冬酶-8优先检测蛋白酶半胱天冬酶-3,并且可在典型MRI研究的15分钟时间范围内检测到。可以使用无响应的PARACEST MRI造影剂作为对照来验证响应。对MEROPS数据库的一项调查表明,这种方法也可用于检测其他蛋白酶,因此可能代表一种用于蛋白酶体研究的新平台技术。