Indrevoll Bård, Kindberg Grete Mørk, Solbakken Magne, Bjurgert Emma, Johansen John Henrik, Karlsen Hege, Mendizabal Marivi, Cuthbertson Alan
GE Healthcare, Medical Diagnostics, Discovery Research, Oslo, Norway.
Bioorg Med Chem Lett. 2006 Dec 15;16(24):6190-3. doi: 10.1016/j.bmcl.2006.09.033. Epub 2006 Sep 26.
Targeting the molecular pathways associated with angiogenesis offers great potential in detecting disease pathology using in vivo imaging technologies. Initiation of angiogenesis requires activation and migration of endothelial cells in order for neovascularization to proceed. Endothelial cells associate with the extracellular matrix through specific interactions with a variety of cell adhesion receptors known as integrins. Peptides containing the tripeptide sequence RGD are known to bind with high affinity to the alphavbeta3 and alphavbeta5 integrins associated with angiogenesis. We present herein the synthesis and in vitro binding affinity of the RGD-containing peptide NC-100717 and a range of molecular probes derived from this intermediate.
靶向与血管生成相关的分子途径在利用体内成像技术检测疾病病理方面具有巨大潜力。血管生成的起始需要内皮细胞的激活和迁移,以便新血管形成得以进行。内皮细胞通过与多种称为整合素的细胞粘附受体的特异性相互作用与细胞外基质结合。已知含有三肽序列RGD的肽与血管生成相关的αvβ3和αvβ5整合素具有高亲和力结合。本文介绍了含RGD肽NC-100717及其一系列衍生自该中间体的分子探针的合成及体外结合亲和力。