Chanda Nripen, Shukla Ravi, Katti Kattesh V, Kannan Raghuraman
Department of Radiology, University of Missouri-Columbia, Columbia, Missouri 65212, USA.
Nano Lett. 2009 May;9(5):1798-805. doi: 10.1021/nl8037147.
Gastrin releasing protein receptor specific bombesin (BBN) peptide-gold nanoconjugates were successfully synthesized using gold nanorods and dithiolated peptide. The gold nanorod-bombesin (GNR-BBN) conjugates showed extraordinary in vitro stabilities against various biomolecules including NaCl, cysteine, histidine, bovine serum albumin, human serum albumin, and dithiothreitol. Quantitative measurements on the binding affinity (IC(50)) of GNR-BBN conjugates toward prostate and breast tumor cells were evaluated. The IC(50) values establish that GNR-BBN conjugates have strong affinity toward the gastrin releasing peptide receptors on both the tumors. Detailed cellular interaction studies of GNR-BBN conjugates revealed that nanorods internalize via a receptor-mediated endocytosis pathway. The receptor specific interactions of GNR-BBN conjugates provide realistic opportunities in the design and development of in vivo molecular imaging and therapy agents for cancer.
利用金纳米棒和二硫醇化肽成功合成了胃泌素释放蛋白受体特异性蛙皮素(BBN)肽-金纳米共轭物。金纳米棒-蛙皮素(GNR-BBN)共轭物对包括氯化钠、半胱氨酸、组氨酸、牛血清白蛋白、人血清白蛋白和二硫苏糖醇在内的各种生物分子表现出非凡的体外稳定性。评估了GNR-BBN共轭物对前列腺和乳腺肿瘤细胞的结合亲和力(IC(50))的定量测量。IC(50)值表明GNR-BBN共轭物对两种肿瘤上的胃泌素释放肽受体具有很强的亲和力。GNR-BBN共轭物的详细细胞相互作用研究表明,纳米棒通过受体介导的内吞途径内化。GNR-BBN共轭物的受体特异性相互作用为癌症体内分子成像和治疗剂的设计与开发提供了切实可行的机会。