Wang Xi-Jie, An Shan-Shan, Cheng Hong, Xu San-Hua, Cheng Jie, Lu Wei, Gao Rong, Xiao Hang
Laboratory of Neurotoxicology, School of Public Health, Nanjing Medical University, Nanjing, Jiangsu, People's Republic China.
J Toxicol Environ Health A. 2009;72(6):359-68. doi: 10.1080/15287390802328945.
A long-chain polypeptide BmKNJX11 was purified from the venom of Asian scorpion Buthus martensi Karsch (BmK) by a combination of gel filtration, ion-exchange chromatography, and reverse-phase high-performance liquid chromatography. The molecular mass was found to be 7036.85 Da by electrospray ionization mass spectrometry. The first 15 N-terminal amino acid sequence of BmKNJX11 was determined to be GRDAY IADSE NCTYT by Edman degradation. With whole cell recording, BmKNJX11 inhibited tetrodotoxin-sensitive voltage-gated sodium channels (TTX-S VGSC) in freshly isolated rat dorsal root ganglion (DRG) neurons in a concentration- and voltage-dependent manner. At a concentration of 40 mug/ml BmKNJX11 lowered the activation threshold and produced negative shifting of TTX-S sodium current (I(Na)) activation curve. In addition, BmKNJX11 induced shifting of the steady-state inactivation curve to the left, delayed the recovery of TTX-S I(Na) from inactivation, and also reduced the fraction of available sodium channels. These results suggested that BmKNJX11 might exert effects on VGSC by binding to a specific site. Considering that TTX-S VGSC expressed in DRG neurons play a critical role in nociceptive transmission, the interaction of BmKNJX11 with TTX-S VGSC might lead to a change in excitability of nociceptive afferent fibers, which may be involved in the observed peripheral pain expression.
通过凝胶过滤、离子交换色谱和反相高效液相色谱相结合的方法,从亚洲钳蝎(Buthus martensi Karsch,BmK)毒液中纯化出一种长链多肽BmKNJX11。通过电喷雾电离质谱法测得其分子量为7036.85道尔顿。通过埃德曼降解法确定BmKNJX11的前15个N端氨基酸序列为GRDAY IADSE NCTYT。采用全细胞记录法,BmKNJX11以浓度和电压依赖性方式抑制新鲜分离的大鼠背根神经节(DRG)神经元中的河豚毒素敏感电压门控钠通道(TTX-S VGSC)。在浓度为40μg/ml时,BmKNJX11降低了激活阈值,并使TTX-S钠电流(I(Na))激活曲线产生负向移位。此外,BmKNJX11使稳态失活曲线向左移位,延迟了TTX-S I(Na)从失活状态的恢复,并且还减少了可用钠通道的比例。这些结果表明,BmKNJX11可能通过与特定位点结合对VGSC发挥作用。鉴于DRG神经元中表达的TTX-S VGSC在伤害性感受传递中起关键作用,BmKNJX11与TTX-S VGSC的相互作用可能导致伤害性传入纤维兴奋性的改变,这可能与观察到的外周疼痛表现有关。