Muller John P E, Aytar Burcu S, Kondo Yukishige, Lynn David M, Abbott Nicholas L
Department of Chemical and Biological Engineering, University of Wisconsin-Madison, 1415 Engineering Drive, Madison, WI 53706, USA.
Soft Matter. 2012 Jan 1;8(24):2608-2619. doi: 10.1039/C2SM00047D. Epub 2012 May 17.
We report small angle X-ray and neutron scattering measurements that reveal that mixtures of the redox-active lipid bis(11-ferrocenylundecyl)dimethylammonium bromide (BFDMA) and dioleoylphosphatidylethanolamine (DOPE) spontaneously form lipoplexes with DNA that exhibit inverse hexagonal nanostructure (H(II) (c)). In contrast to lipoplexes of DNA and BFDMA only, which exhibit a multilamellar nanostructure (L(α) (c)) and limited ability to transfect cells in the presence of serum proteins, we measured lipoplexes of BFDMA and DOPE with the H(II) (c) nanostructure to survive incubation in serum and to expand significantly the range of media compositions (e.g., up to 80% serum) over which BFDMA can be used to transfect cells with high efficiency. Importantly, we also measured the oxidation state of the ferrocene within the BFDMA/DNA lipoplexes to have a substantial influence on the transfection efficiency of the lipoplexes in media containing serum. Specifically, whereas lipoplexes of reduced BFDMA and DOPE transfect cells with high efficiency, lipoplexes of oxidized BFDMA and DNA lead to low levels of transfection. Complementary measurements using SAXS reveal that the low transfection efficiency of the lipoplexes of oxidized BFDMA and DOPE correlates with the presence of weak Bragg peaks and thus low levels of H(II) (c) nanostructure in solution. Overall, these results provide support for our hypothesis that DOPE-induced formation of the H(II) (c) nanostructure of the BFDMA-containing lipoplexes underlies the high cell transfection efficiency measured in the presence of serum, and that the oxidation state of BFDMA within lipoplexes with DOPE substantially regulates the formation of the H(II) (c) nanostructure and thus the ability of the lipoplexes to transfect cells with DNA. More generally, the results presented in this paper suggest that lipoplexes formed from BFDMA and DOPE may offer the basis of approaches that permit active and external control of transfection of cells in the presence of high (physiologically relevant) levels of serum.
我们报告了小角X射线和中子散射测量结果,这些结果表明,氧化还原活性脂质双(11-二茂铁基十一烷基)二甲基溴化铵(BFDMA)与二油酰磷脂酰乙醇胺(DOPE)的混合物能与DNA自发形成具有反六角纳米结构(H(II) (c))的脂质体复合物。与仅由DNA和BFDMA形成的具有多层纳米结构(L(α) (c))且在血清蛋白存在下转染细胞能力有限的脂质体复合物不同,我们测量发现具有H(II) (c)纳米结构的BFDMA和DOPE脂质体复合物在血清中孵育后仍能存活,并且显著扩大了BFDMA可用于高效转染细胞的培养基成分范围(例如,高达80%血清)。重要的是,我们还测量发现BFDMA/DNA脂质体复合物中二茂铁的氧化态对脂质体复合物在含血清培养基中的转染效率有重大影响。具体而言,还原态BFDMA和DOPE的脂质体复合物能高效转染细胞,而氧化态BFDMA和DNA的脂质体复合物导致的转染水平较低。使用小角X射线散射(SAXS)的补充测量表明,氧化态BFDMA和DOPE脂质体复合物的低转染效率与弱布拉格峰的存在相关,因此溶液中H(II) (c)纳米结构水平较低。总体而言,这些结果支持了我们的假设,即DOPE诱导含BFDMA脂质体复合物形成H(II) (c)纳米结构是在血清存在下测得的高细胞转染效率的基础,并且与DOPE形成脂质体复合物时BFDMA的氧化态实质上调节了H(II) (c)纳米结构的形成,从而也调节了脂质体复合物用DNA转染细胞的能力。更一般地说,本文给出的结果表明,由BFDMA和DOPE形成的脂质体复合物可能为在高(生理相关)血清水平存在下允许对细胞转染进行主动和外部控制的方法提供基础。