全合成脂肽基因载体转染剂的DNA缩合研究

Tarwadi Tarwadi, H. Rachmawati, R. E. Kartasasmita, S. Pambudi, A. D. Arbianto, D. Restiani, Sukmadjaja Asyarie
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引用次数: 0

摘要

转染剂的主要要求是将DNA浓缩到纳米颗粒大小,保护DNA在细胞质和细胞核中运输过程中不受核酸酶和其他降解酶的影响,并且对靶细胞无毒。本研究设计合成了棕榈酰(C-16)和短肽序列组成的脂肽,并对其DNA缩聚能力和毒性进行了测试。DNA缩聚研究采用EtBr排除法,细胞毒性测定采用比色MTT法。结果表明,基于脂肽的Pal-CKKHH和Pal-CKKHH- ygrkkrrqrrr - pkkkrkv转染剂能有效地凝聚DNA分子。与脂质胺和聚l-赖氨酸相比,脂肽的毒性更小,这表明当4.36µM Pal-CKKHHYGRKKRRQRRR-PKKKRKV处理CHO-K1细胞时,90%的CHO-K1细胞仍然存活。同时,用PLL和Lipofectamine®2000处理CHO-K1时,分别只有~75%和80%的活细胞。此外,2.18µM Pal-CKKHH-YGRKKRRQRRR-PKKKRKV处理后,HepG2细胞存活率为~ 75%,而当脂肽浓度增加到8.72 M时,HepG2细胞存活率下降至~65%。总之,合成的脂肽能有效凝聚DNA分子,毒性低于Lipofectamine®2000和PLL,有可能作为非病毒基因传递载体进行探索。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
DNA Condensation Study of Fully Synthesized Lipopeptide-Based Transfection Agent for Gene Delivery Vehicle
   The main requirement of transfection agent has to condense DNA in nanoparticle size, protect the DNA from nucleases and other degrading enzymes during its transport in cell cytoplasm and nucleus and should not toxic to target cells. In this research, lipopeptide composed of palmitoyl (C-16) and short peptide sequence have been designed fully synthesized and tested to DNA condensation capability and toxicity. The DNA condensation study was performed using EtBr exclusion assay and cytotoxicity determination was carried out by colorimetric MTT assay. It was revealed that lipopeptide-based transfection agent of Pal-CKKHH and Pal-CKKHH-YGRKKRRQRRR-PKKKRKV condensed DNA molecules efficiently. The lipopeptide was less toxic compared to Lipofectamine and Poly-L-Lysine, that shown by 90% of CHO-K1 cells remained viable when they were treated with 4.36 µM Pal-CKKHHYGRKKRRQRRR-PKKKRKV. Meanwhile, there were only ~75% and 80% of CHO-K1 viable cells when it was treated with PLL and Lipofectamine®2000, respectively. Moreover, cell viability of HepG2 was ~ 75% after treated with 2.18 µM of Pal-CKKHH-YGRKKRRQRRR-PKKKRKV and decreased to ~65% when the lipopeptide concentration increased to 8.72 M. In summary, the synthesized lipopeptide condenses DNA molecules efficiently, less toxic than Lipofectamine®2000 and PLL and has possibility to be explored as a non-viral gene delivery vehicle.
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