Belozersky Institute of Physico-Chemical Biology, Lomonosov Moscow State University, Moscow, 119992, Russia.
Biochemistry (Mosc). 2009 Sep;74(9):1021-6. doi: 10.1134/s0006297909090107.
A study of the properties of water-soluble tetrasubstituted cationic aluminum phthalocyanine (AlPcN(4)) revealed efficient binding of this photosensitizer to phospholipid membranes as compared with tetrasulfonated aluminum and zinc phthalocyanine complexes. This also manifested itself in enhanced photodynamic activity of AlPcN(4) as measured by the photosensitized damage of gramicidin channels in a planar bilayer lipid membrane. The largest difference in the photodynamic activity of cationic and anionic phthalocyanines was observed in a membrane containing negatively charged lipids, thereby pointing to significant contribution of electrostatic interactions to the binding of photosensitizers to a membrane. Fluoride anions suppressed the photodynamic activity and binding to membrane of both tetraanionic and tetracationic aluminum phthalocyanines, which supports our hypothesis that interaction of charged metallophthalocyanines with phospholipid membranes is mostly determined by coordination of the central metal atom with the phosphate group of lipid.
水溶性四取代正离子型铝酞菁(AlPcN(4))的性质研究表明,与四磺酸基取代的铝和锌酞菁配合物相比,该光敏剂与磷脂膜具有更强的结合能力。这一点也表现在 AlPcN(4) 的光动力活性增强上,通过平面双层脂质膜中革兰氏菌素通道的光致敏损伤来衡量。在含有带负电荷的脂质的膜中,观察到正离子型和负离子型酞菁的光动力活性的最大差异,从而表明静电相互作用对光敏剂与膜的结合有重要贡献。氟离子抑制了四阴离子型和四正离子型铝酞菁的光动力活性和与膜的结合,这支持了我们的假设,即带电荷的金属酞菁与磷脂膜的相互作用主要取决于中心金属原子与脂质磷酸基团的配位。