Kirilenko Aneta, Golczak Marcin, Pikula Slawomir, Buchet Rene, Bandorowicz-Pikula Joanna
Department of Cellular Biochemistry, Nencki Institute of Experimental Biology, 02-093 Warsaw, Poland.
Biophys J. 2002 May;82(5):2737-45. doi: 10.1016/S0006-3495(02)75614-2.
Annexin VI (AnxVI) formed ion channels in planar lipid bilayers that were induced by the addition of millimolar guanosine 5'-triphosphate (GTP) at pH 7.4 and that were not accompanied by a penetration of the protein into the membrane hydrophobic region. GTP-influenced interactions of AnxVI with Ca2+/liposomes produced small structural alterations as revealed by circular dichroism and infrared spectroscopies. Guanosine 5'-3-O-(thio)-triphosphate (GTPgammaS) binding to AnxVI, promoted by the photorelease of GTPgammaS from GTPgammaS[1-(4,5-dimethoxy-2-nitrophenyl)-ethyl] (caged-GTPgammaS), affected three to four amino acid residues of AnxVI in the presence of Ca2+/liposomes, while about eight or nine amino acid residues were altered in their absence. This suggested that the nucleotide-binding site overlapped the lipid-binding domain of AnxVI. The binding of the fluorescent GTP analog, 2'-(or 3')-O-(2,4,6-trinitrophenyl)guanosine 5'-triphosphate (TNP-GTP) to AnxVI was optimal in the presence of Ca2+/liposomes, with a dissociation constant (K(d)) of 1 microM and stoichiometry of 1. TNP-GTP promoted fluorescence resonance energy transfer from tryptophan residues to the nucleotide. Ion conductance and fluorescence measurements of the C- and N-terminal fragments of AnxVI indicated distinct GTP-binding properties, suggesting that the existence of the GTP-induced ion channel activity of AnxVI is associated with the flexibility of the two halves of the protein. Such structural flexibility could contribute to a molecular mechanism of AnxVI acting as a GTP biosensor.
膜联蛋白VI(AnxVI)在平面脂质双分子层中形成离子通道,该通道在pH 7.4时由加入毫摩尔浓度的鸟苷5'-三磷酸(GTP)诱导形成,且蛋白质不会穿透到膜疏水区域。圆二色光谱和红外光谱显示,GTP影响AnxVI与Ca2+/脂质体的相互作用,产生微小的结构变化。鸟苷5'-3-O-(硫代)-三磷酸(GTPγS)与AnxVI的结合,由GTPγS[1-(4,5-二甲氧基-2-硝基苯基)-乙基](笼形GTPγS)的光释放促进,在Ca2+/脂质体存在时影响AnxVI的三到四个氨基酸残基,而在不存在时约有八个或九个氨基酸残基发生改变。这表明核苷酸结合位点与AnxVI的脂质结合结构域重叠。荧光GTP类似物2'-(或3')-O-(2,4,6-三硝基苯基)鸟苷5'-三磷酸(TNP-GTP)与AnxVI的结合在Ca2+/脂质体存在时最佳,解离常数(K(d))为1 microM,化学计量比为1。TNP-GTP促进从色氨酸残基到核苷酸的荧光共振能量转移。AnxVI C端和N端片段的离子电导和荧光测量表明具有不同的GTP结合特性,这表明AnxVI的GTP诱导离子通道活性的存在与蛋白质两半部分的灵活性有关。这种结构灵活性可能有助于AnxVI作为GTP生物传感器的分子机制。