Wu C Y, Chen W C, Ho C L, Chen S T, Wang K T
Institute of Biological Chemistry, Academia Sinica, Taipei, Taiwan, Republic of China.
Biochem Biophys Res Commun. 1997 Apr 28;233(3):713-6. doi: 10.1006/bbrc.1997.6503.
The N-terminal leucine residue of snake venom cardiotoxin II (CTX II) (Naja naja atra) was systematically replaced with D-leucine (CTXII-L1-D-L), glycine (CTXII-L1G) or deleted [CTXII-(2-60)] to study the role of leucine residue in CTX II molecule. CTX II, CTXL1-D-L, CTXL1G and CTX(2-60) were produced by chemical synthesis method and purified by high performance liquid chromatography. Owing to folding problem in CTXII-(2-60), only CTX II, CTXII-L1-D-L and CTXII-L1G were produced in a pure form and characterized by amino acid analysis, mass spectrometry and peptide mapping. In the structural aspect, changing the Leu-1 by D-Leu or Gly causes a drastic alteration in the whole CTX II structure as detected by circular dichroism, 1-anilino-naphthalene-8-sulfonate (ANS) fluorescence assay. In the functional aspect, both CTXII-L1-D-L and CTXII-L1G are still retained substantial biological activity of CTX II. Therefore, the results indicate that both the chirality and the side-chain of the N-terminal leucine residue of CTX II are important elements in maintaining the whole CTX II structure. In addition, this study is the first report in elucidating the reason why the first N-terminal residue of most CTXs (90.3%) is leucine residue.
系统地将蛇毒心脏毒素II(CTX II)(中华眼镜蛇)的N端亮氨酸残基替换为D-亮氨酸(CTXII-L1-D-L)、甘氨酸(CTXII-L1G)或删除该残基[CTXII-(2-60)],以研究亮氨酸残基在CTX II分子中的作用。CTX II、CTXII-L1-D-L、CTXII-L1G和CTX(2-60)采用化学合成法制备,并通过高效液相色谱法纯化。由于CTXII-(2-60)存在折叠问题,只有CTX II、CTXII-L1-D-L和CTXII-L1G以纯形式制备,并通过氨基酸分析、质谱和肽图分析进行表征。在结构方面,通过圆二色性、1-苯胺基萘-8-磺酸盐(ANS)荧光测定法检测到,用D-亮氨酸或甘氨酸取代Leu-1会导致整个CTX II结构发生剧烈变化。在功能方面,CTXII-L1-D-L和CTXII-L1G仍保留了CTX II的大量生物活性。因此,结果表明,CTX II的N端亮氨酸残基的手性和侧链都是维持整个CTX II结构的重要元素。此外,本研究首次报道了阐明大多数CTXs(90.3%)的第一个N端残基为亮氨酸残基的原因。