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Erratum to: Peptide radiopharmaceuticals for diagnosis and therapy.《用于诊断和治疗的肽类放射性药物》勘误
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2
A dual-labeled knottin peptide for PET and near-infrared fluorescence imaging of integrin expression in living subjects.一种用于活体受试者中整合素表达的正电子发射断层扫描(PET)和近红外荧光成像的双标记结蛋白肽。
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3
Evaluation of a (64)Cu-labeled cystine-knot peptide based on agouti-related protein for PET of tumors expressing alphavbeta3 integrin.基于 agouti 相关蛋白的半胱氨酸结肽用于检测表达 alphavbeta3 整合素的肿瘤的 PET 研究:(64)Cu 标记半胱氨酸结肽的评价。
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An engineered knottin peptide labeled with 18F for PET imaging of integrin expression.一种用 18F 标记的工程化 knottin 肽,用于整合素表达的 PET 成像。
Bioconjug Chem. 2009 Dec;20(12):2342-7. doi: 10.1021/bc900361g.
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Biosynthesis and biological screening of a genetically encoded library based on the cyclotide MCoTI-I.基于环肽MCoTI-I的基因编码文库的生物合成与生物筛选
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64Cu-labeled affibody molecules for imaging of HER2 expressing tumors.64Cu 标记的亲和体分子用于 HER2 表达肿瘤的成像。
Mol Imaging Biol. 2010 Jun;12(3):316-24. doi: 10.1007/s11307-009-0256-6. Epub 2009 Sep 25.
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Potent inhibitors of beta-tryptase and human leukocyte elastase based on the MCoTI-II scaffold.基于MCoTI-II支架的β-胰蛋白酶和人白细胞弹性蛋白酶的强效抑制剂。
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Changes in HER2 expression in breast cancer xenografts after therapy can be quantified using PET and (18)F-labeled affibody molecules.治疗后乳腺癌异种移植瘤中HER2表达的变化可以使用PET和(18)F标记的亲和体分子进行定量。
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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.

DOI:10.1007/s00726-010-0503-9
PMID:20174842
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2914822/
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。