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基于蛋白质支架的癌症分子成像分子探针。

Protein scaffold-based molecular probes for cancer molecular imaging.

机构信息

Department of Radiology, Molecular Imaging Program at Stanford, Stanford University, CA 94305-5344, USA.

出版信息

Amino Acids. 2011 Nov;41(5):1037-47. doi: 10.1007/s00726-010-0503-9. Epub 2010 Feb 21.

Abstract

Protein scaffold molecules are powerful reagents for targeting various cell signal receptors, enzymes, cytokines and other cancer-related molecules. They belong to the peptide and small protein platform with distinct properties. For the purpose of development of new generation molecular probes, various protein scaffold molecules have been labeled with imaging moieties and evaluated both in vitro and in vivo. Among the evaluated probes Affibody molecules and analogs, cystine knot peptides, and nanobodies have shown especially good characteristics as protein scaffold platforms for development of in vivo molecular probes. Quantitative data obtained from positron emission tomography, single photon emission computed tomography/CT, and optical imaging together with biodistribution studies have shown high tumor uptakes and high tumor-to-blood ratios for these probes. High tumor contrast imaging has been obtained within 1 h after injection. The success of those molecular probes demonstrates the adequacy of protein scaffold strategy as a general approach in molecular probe development.

摘要

蛋白质支架分子是靶向各种细胞信号受体、酶、细胞因子和其他癌症相关分子的有力试剂。它们属于具有独特性质的肽和小蛋白平台。为了开发新一代分子探针,已经将各种蛋白质支架分子标记成像部分,并在体外和体内进行了评估。在评估的探针中,亲和体分子和类似物、半胱氨酸结肽和纳米抗体作为体内分子探针开发的蛋白质支架平台表现出特别好的特性。正电子发射断层扫描、单光子发射计算机断层扫描/计算机断层扫描和光学成像获得的定量数据以及生物分布研究表明,这些探针具有高肿瘤摄取率和高肿瘤与血液的比值。在注射后 1 小时内即可获得高肿瘤对比度成像。这些分子探针的成功证明了蛋白质支架策略作为分子探针开发的一般方法是可行的。

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