敬钊毒素-Ⅰ(JZTX-Ⅰ)是一种能够抑制心肌钠通道失活的新型蜘蛛神经毒素,该文结合高效液相色谱与色氨酸荧光测定技术研究了JZTX-Ⅰ的磷脂膜结合活性.脂质体共沉淀实验表明,JZTX-Ⅰ具有不依赖于带负电荷磷脂组成的生物膜结合活性.当加入由酸性或中性磷脂构成的脂质体后,JZTX-Ⅰ能够分别产生6.4和4.7 nm的蓝移以及7.4和8.0 nm的红移激发漂移,显示JZTX-Ⅰ能够插入磷脂膜,同时该分子疏水表面的色氨酸残基处于一个运动受限的界面区域.荧光淬灭实验进一步证实,与脂质体结合能够减少该毒素分子表面色氨酸残基的溶剂暴露.该研究结果为阐明JZTX-Ⅰ的离子通道门控调节机制提供了新的信息.
参考文献
[1] | Vais H,Williamson M S,Goodson S J,Devonshire A L,Warmke J W,Usherwood P N R,Cohen C J.J Gen Physiol,2000,115:305 |
[2] | Catterall W A.Neuron,2000,26:13 |
[3] | Cummins T R,Aglieco F,Dib-Hajj S D.Mol Pharmacol,2002,61:1 192 |
[4] | Middleton R E,Warren V A,Kraus R L,Hwang J C,Liu C J,Dai G,Brochu R M,Kohler M G,Gao Y D,Garsky V M,et al.Biochemistry,2002,41:14 734 |
[5] | Takahashi H,Kim J I,Min H J,Sato K,Swartz K J,Shimada I.J Mol Biol,2000,297:771 |
[6] | Benzinger G R,Kyle J W,Blumenthal K M,Hanck D A.J Biol Chem,1998,273:80 |
[7] | Lee S Y,MacKinnon R.Nature,2004,430:232 |
[8] | Suchyna T M,Tape S E,Koeppe R E,Andersen O S,Sachs F,Gottlieb P A.Nature,2004,430:235 |
[9] | Smith J J,Alphy S,Seibert A L,Blumenthal K M.J Biol Chem,2005,280:11 127 |
[10] | Phillips L R,Milescu M,Li-Smerin Y Y,Mindell J A,Kim J I,Swartz K J.Nature,2005,436:857 |
[11] | Xiao Y C,Tang J Z,Hu W J,Xie J Y,Maertens C,Tytgat J,Liang S P.J Biol Chem,2005,280(13):12 069 |
[12] | Wieprecht T,Apostolov O,Seelig J.Biophys Chem,2000,85:187 |
[13] | Ladokhin A S,Jayasinghe S,White S H.Anal Biochem,2000,285:235 |
[14] | Falls L A,Furie B C,Jacobs M,Furie B,Rigby A C.J Biol Chem,2001,276:23 895 |
[15] | Jung H J,Lee J Y,Kim S H,Eu Y J,Shin S Y,Milescu M,Swartz K J,Kim J I.Biochemistry,2005,44:6 015 |
[16] | Goudet C,Huys I,Clynen E,Schoofs L,Wang D C,Waelkens E,Tytgat J.FEBS Letters,2001,495:61 |
[17] | Xiao Y C,Liang S P.Eur J Pharmacol,2003,477:1 |
[18] | Sun Y M,Bosmans F,Zhu R H,Goudet C,Xiong Y M,Tytgat J,Wang D C.J Biol Chem,2003,278(26):24 125 |
[19] | Szeto T H,Birinyi-Strachan L C,Smith R,Connor M,Christie M J,King G F,Nicholson G M.FEBS Lett,2000,470:293 |
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