Ahmed T, Kelly S M, Lawrence A J, Mezna M, Price N C
University of Glasgow, UK.
J Biochem. 1996 Dec;120(6):1224-31. doi: 10.1093/oxfordjournals.jbchem.a021545.
Bee venom PLA2 possesses a binding site for long-chain fatty acids that can be acylated by long-chain fatty acid imidazolides [Drainas, D. and Lawrence, A.J. (1978) Eur. J. Biochem. 91, 131-138]. Occupation of the site either by oleic acid or the oleoyl residue enhances the catalytic activity by 45.7-fold in the presence of 20% 1-propanol and occupation of the site by the oleoyl residue increases the lytic activity against rabbit erythrocytes by 60-fold. Treatment of the enzyme with oleic acid and glutaraldehyde is known to produce irreversible activation [Lawrence, A.J. and Moores, G.R. (1975) FEBS Lett. 49, 287-291]. Here we show that reduction of the glutaraldehyde-treated enzyme with borohydride stabilizes the activated state and enables the fatty acid to be removed, revealing that a large proportion of the induced activation does not require the presence of oleic acid and indicating that activation is due to a change in the conformation rather than the hydrophobicity of the protein. A kinetic study of enzyme activated by oleoyl imidazolide showed that this modification stabilizes the protein against reversible inactivation by 1-propanol. Comparison of the CD spectra of native and oleoyl imidazolide-activated enzyme shows a change in secondary structure with apparent increase in both alpha-helix and beta-sheet content. During reaction of the enzyme with oleoyl imidazolide, the protein fluorescence shows a biphasic response with an initial fall attributed to occupation of the binding site followed by a progressive decrease with a shift of the emission maximum from 341 to 348 nm. The rate of the second phase closely matched the rate of increase in catalytic activity of the enzyme. Free oleic acid caused a rapid fall in fluorescence emission without the subsequent slow change. These results support the proposal that oleic acid or the oleoyl residue occupy a very similar site on the protein and that occupation of this site increases the exposure of one or both of the Trp residues to the aqueous environment. Binding studies show that activation by oleoyl imidazolide does not increase the affinity of the enzyme for the erythrocyte membrane. It is proposed that occupation of a long-chain fatty acid binding site on the enzyme enhances catalytic activity by changing the conformation of the protein rather than acting as a hydrophobic anchor to the substrate surface.
蜂毒磷脂酶A2具有一个可被长链脂肪酸咪唑化物酰化的长链脂肪酸结合位点[德雷纳斯,D.和劳伦斯,A.J.(1978年)《欧洲生物化学杂志》91卷,第131 - 138页]。油酸或油酰基占据该位点会在20% 1 - 丙醇存在的情况下使催化活性提高45.7倍,而油酰基占据该位点会使对兔红细胞的溶血活性提高60倍。已知用油酸和戊二醛处理该酶会产生不可逆激活[劳伦斯,A.J.和穆尔斯,G.R.(1975年)《欧洲生物化学学会联合会快报》49卷,第287 - 291页]。在此我们表明,用硼氢化钠还原经戊二醛处理的酶可稳定激活状态并能去除脂肪酸,这表明大部分诱导激活并不需要油酸的存在,且表明激活是由于蛋白质构象的改变而非其疏水性的改变。对用油酰基咪唑化物激活的酶进行的动力学研究表明,这种修饰可使蛋白质稳定,防止被1 - 丙醇可逆失活。天然酶和油酰基咪唑化物激活的酶的圆二色光谱比较显示二级结构发生了变化,α - 螺旋和β - 折叠含量明显增加。在酶与油酰基咪唑化物反应过程中,蛋白质荧光呈现双相响应,最初的下降归因于结合位点被占据,随后随着发射最大值从341纳米移至348纳米而逐渐降低。第二阶段的速率与酶催化活性增加的速率紧密匹配。游离油酸导致荧光发射迅速下降,随后没有缓慢变化。这些结果支持了这样的观点,即油酸或油酰基在蛋白质上占据非常相似的位点,且该位点的占据增加了一个或两个色氨酸残基对水环境的暴露。结合研究表明,油酰基咪唑化物激活并不会增加酶对红细胞膜的亲和力。有人提出,酶上长链脂肪酸结合位点的占据通过改变蛋白质构象而非作为底物表面的疏水锚来增强催化活性。