Kawano Takahito, Murata Masaharu, Piao Jing Shu, Narahara Sayoko, Hamano Nobuhito, Kang Jeong-Hun, Hashizume Makoto
Innovation Center for Medical Redox Navigation, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka 812-8582, Japan.
Department of Advanced Medical Initiatives, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka 812-8582, Japan.
Int J Mol Sci. 2014 Dec 24;16(1):148-58. doi: 10.3390/ijms16010148.
Matrix metalloproteinase 2 (MMP-2) in metastatic cancer tissue, which is associated with a poor prognosis, is a potential target for tumor imaging in vivo. Here, we describe a metastatic cancer cell-targeted protein nanocage. An MMP-2-binding peptide, termed CTT peptide (CTTHWGFTLC), was conjugated to the surface of a naturally occurring heat shock protein nanocage by genetic modification. The engineered protein nanocages showed a binding affinity for MMP-2 and selective uptake in cancer cells that highly expressed MMP-2 in vitro. In near-infrared fluorescence imaging, the nanocages showed specific and significant accumulation in tumor tissue after intravenous injection in vivo. These protein nanocages conjugated with CTT peptide could be potentially applied to a noninvasive near-infrared fluorescence detection method for imaging gelatinase activity in metastatic tumors in vivo.
基质金属蛋白酶2(MMP - 2)存在于转移性癌组织中,与预后不良相关,是体内肿瘤成像的潜在靶点。在此,我们描述了一种靶向转移性癌细胞的蛋白质纳米笼。一种名为CTT肽(CTTHWGFTLC)的MMP - 2结合肽通过基因修饰与天然存在的热休克蛋白纳米笼表面偶联。工程化的蛋白质纳米笼在体外对MMP - 2表现出结合亲和力,并能被高表达MMP - 2的癌细胞选择性摄取。在近红外荧光成像中,纳米笼在体内静脉注射后在肿瘤组织中显示出特异性且显著的聚集。这些与CTT肽偶联的蛋白质纳米笼可能潜在地应用于一种非侵入性近红外荧光检测方法,用于体内转移性肿瘤中明胶酶活性的成像。