2023年第50卷第9期目录
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封面故事:近年来,因具有基因沉默等功能,脱氧核酶受到越来越多的关注,但受带负电荷和亲
水性的影响,其难以通过细胞膜进入细胞,导致催化切割效率严重降低,限制了在临床治疗方面
的应用。我们前期应用SELEX技术筛选出肝癌细胞特异性膜蛋白VASN的特异核酸适配体V4-2,并
发现其具有跨细胞膜递送的潜能。基于此,本文将核酸适配体V4-2与靶向端粒酶逆转录酶的脱氧
核酶(Dz) 偶联,形成具有靶RNA切割活性的偶联物V4-2-Dz。进一步研究结果表明,V4-2-Dz具
有靶向肝癌细胞内递送和脱氧核酶底物切割活性。本研究为脱氧核酶的细胞靶向和跨膜递送提供
了一种新的思路。
(马斐越,李慧,刘雪梅,台福敏,邵宁生,高波,郑晓飞. VASN核酸适配体与端粒酶逆转录
酶脱氧核酶偶联物的生物学功能研究,本期第2175~2184 页)
Cover Story:Objective To investigate the target RNA cleavage activity of V4-2-Dz a conjugate formed by coupling the aptamer V4-2 of the hepatocellular carcinoma cell-specific membrane protein VASN (vasorin) with the DNAzyme (Dz) targeting the telomerase reverse transcriptase (hTERT), in vitro and in hepatocellular carcinoma cells, and to establish a new strategy for DNAzyme delivery.Methods The secondary structure of V4-2-Dz was predicted by using the Mfold website and the cleavage activity of V4-2-Dz was examined by in vitro cleavage assay. And then, the ability of V4-2-Dz binding to hepatocellular carcinoma HepG2 cells was examined by flow cytometry and laser confocal assay. The effects of V4-2-Dz on the hTERT mRNA expression and cell proliferation of HepG2 cells were analyzed by using RT-qPCR and MTT assays.Results In vitro cleavage assays showed that V4-2-Dz has hTERT RNA cleavage activity. Flow cytometry and laser confocal results showed that V4-2-Dz specifically binds to HepG2 cells and could reduce the hTERT mRNA levels and inhibit cell proliferation significantly.Conclusion The conjugate of aptamer V4-2 with DNAzyme of telomerase reverse transcriptase, V4-2-Dz, has targeted cellular delivery and cleavage activity. The conjugate based on the aptamer and DNazyme provides a new idea for antitumor drug research.
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核酸适配体技术研究专刊
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