Ho C L, Shih Y P, Wang K T, Yu H M
Institute of Biological Chemistry, Academia Sinica, Nankang, Taipei 115, Taiwan.
Toxicon. 2001 Oct;39(10):1561-6. doi: 10.1016/s0041-0101(01)00128-3.
Mastoparan B (MP-B) is a cationic tetradecapeptide (LKLKSIVSWAKKVL-CONH(2)) isolated from the venom of the Taiwan hornet Vespa basalis. Unlike other vespid mastoparans, the peptide is capable of inducing short-term hypotension and causes hemolysis in animals. This study was aimed to find out MP-B analogs that possess higher hypotensive potency with the least lytic action by D-amino acid substitution, especially at lysine (Lys) residues. The synthetic MP-B isomer in which Lys(2) was replaced by D-Lys showed a significant decrease in both hemolytic and hypotensive activities. Substitution of Lys(4) by D-Lys in MP-B also caused a marked reduction of hemolytic activity, but its hypotensive action was only slightly affected. However, when Lys(11,12) were replaced by D-Lys, the resulting isomer ([D-Lys(11,12)]MP-B) exhibited a higher hypotensive activity with negligible hemolytic activity as compared with the native peptide. The D-antipot of MP-B in which all amino acid residues were replaced by D-isomers showed the highest hypotensive activity with a hemolytic activity about 1/5 that of MP-B. The results reveal that D-Lys substitution at the N-terminus of MP-B (Lys(2,4)) causes decreases in both hypotensive and hemolytic activities, while D-Lys substitution at the C-terminus (Lys(11,12)) leads to a significant increase in hypotensive activity of MP-B with a remarkable decrease in hemolytic activity. The hypotensive effect of [D-Lys(11,12)]MP-B was more prominent on spontaneously hypertensive rats. At a proper dose (0.3mg/kg) the peptide could reduce the high blood pressure (approximately 180 mmHg) of the rat to a normal level (approximately 120 mmHg) for more than 3h. [D-Lys(11,12)]MP-B which possesses a potent hypotensive action with the least cytolytic side effect is the best MP-B analog for studying the mechanism of cardiovascular inhibition by MP-B and could be useful as a hypotensive agent in hypertension crisis.
蜂毒肽B(MP - B)是一种阳离子十四肽(LKLKSIVSWAKKVL - CONH₂),从台湾胡蜂黄蜂的毒液中分离得到。与其他胡蜂蜂毒肽不同,该肽能够引起短期低血压,并导致动物溶血。本研究旨在通过D - 氨基酸取代,特别是赖氨酸(Lys)残基的取代,找到具有更高降压效力且溶血作用最小的MP - B类似物。用D - Lys取代Lys₂的合成MP - B异构体在溶血和降压活性方面均显著降低。在MP - B中用D - Lys取代Lys₄也导致溶血活性明显降低,但其降压作用仅略有影响。然而,当Lys₁₁,₁₂被D - Lys取代时,所得异构体([D - Lys₁₁,₁₂]MP - B)与天然肽相比表现出更高的降压活性,溶血活性可忽略不计。所有氨基酸残基都被D - 异构体取代的MP - B的D - 反式异构体表现出最高的降压活性,溶血活性约为MP - B的1/5。结果表明,在MP - B的N端(Lys₂,₄)进行D - Lys取代会导致降压和溶血活性均降低,而在C端(Lys₁₁,₁₂)进行D - Lys取代会导致MP - B的降压活性显著增加,溶血活性显著降低。[D - Lys₁₁,₁₂]MP - B对自发性高血压大鼠的降压作用更为显著。在适当剂量(0.3mg/kg)下,该肽可将大鼠的高血压(约180 mmHg)降至正常水平(约120 mmHg)超过3小时。[D - Lys₁₁,₁₂]MP - B具有强大的降压作用且细胞溶解副作用最小,是研究MP - B心血管抑制机制的最佳MP - B类似物,可作为高血压危象中的降压药物。