Wang Hao, Shi Pei-Ji, Wu Ming-Fen, Li Ning, Zhou Xiao-Liang, Fan Fei-Yue
Institute of Radiation Medicine, Peking Union Medical College and Chinese Academy of Medical Sciences, 300192 Tianjin, China.
Protein Pept Lett. 2010 Dec;17(12):1562-5. doi: 10.2174/0929866511009011562.
Antibody-directed enzyme prodrug therapy (ADEPT) delivers chemotherapeutic agents at high concentration to tumor tissues while minimizing systemic drug exposure. β-Lactamases are particularly useful enzymes for ADEPT systems due to their unique substrate specificity, which allows the activation of a variety of lactam-based prodrugs with minimal interference from mammalian enzymes. This study used integrin α(v)β(3) as a target for tumor-specific delivery of β-Lactamase. β-Lactamase was fused with ACDCRGDCFCG peptide (RGD4C) by recombinant DNA technology. Likewise, this study cloned a fused cDNA and successfully expressed active recombinant protein in E. coli purified with Ni-NTA resin. After purification, β-Lactamase moiety showed the expected size of 42 kDa on Tricine-SDS-PAGE, and was further confirmed by Western blotting. Based on flow cytometric analysis, the purified protein was found to be active for specificity in breast cancer cell line, MCF-7, which supports the utility of the protein as an agent for ADEPT.
抗体导向酶前药疗法(ADEPT)可将化疗药物高浓度地递送至肿瘤组织,同时使全身药物暴露降至最低。由于β-内酰胺酶具有独特的底物特异性,能够在哺乳动物酶的干扰最小的情况下激活多种基于内酰胺的前药,因此它是ADEPT系统中特别有用的酶。本研究将整合素α(v)β(3)用作β-内酰胺酶肿瘤特异性递送的靶点。通过重组DNA技术将β-内酰胺酶与ACDCRGDCFCG肽(RGD4C)融合。同样,本研究克隆了一个融合cDNA,并在经镍-氮三乙酸树脂纯化的大肠杆菌中成功表达了活性重组蛋白。纯化后,β-内酰胺酶部分在Tricine-SDS-PAGE上显示出预期的42 kDa大小,并通过蛋白质印迹进一步证实。基于流式细胞术分析,发现纯化后的蛋白对乳腺癌细胞系MCF-7具有特异性活性,这支持了该蛋白作为ADEPT药物的实用性。