Hasselbach W, Taugner G
Biochem J. 1970 Sep;119(2):265-71. doi: 10.1042/bj1190265.
The thiol groups of the vesicular protein of bovine adrenal medulla were allowed to react with the bifunctional thiol reagent bis-(N-maleimidomethyl) ether and with the monofunctional thiol reagent N-ethylmaleimide, and the ATP-dependent and -independent catecholamine fluxes of the modified preparations were studied. 1. During the initial phase of the reaction bis-(N-maleimidomethyl) ether blocks twice as many thiol groups as does N-ethylmaleimide at equimolar concentrations. 2. Labelling of the bis-(N-maleimidomethyl) ether-protein compound with [(14)C]-cysteine shows that 70-80% of the blocked thiol groups are interconnected by the bifunctional thiol reagent. 3. At a low extent of reaction (1.5mol of thiol groups/10(6)g of protein) the catecholamine efflux is diminished. If more than 2mol of thiol groups/10(6)g of protein are blocked, the efflux is enhanced whichever thiol reagent is applied. 4. If 2-4mol of thiol groups/10(6)g of protein are blocked the inhibition of the catecholamine influx increases linearly with the proportion of the thiol groups blocked. 5. ATP protects the catecholamine influx and the adenosine triphosphatase activity against bis-(N-maleimidomethyl) ether poisoning somewhat less effectively than against N-ethylmaleimide poisoning.
使牛肾上腺髓质囊泡蛋白的巯基与双功能巯基试剂双 -(N - 马来酰亚胺甲基)醚和单功能巯基试剂N - 乙基马来酰亚胺反应,并研究修饰制剂的ATP依赖性和非依赖性儿茶酚胺通量。1. 在反应初始阶段,等摩尔浓度下双 -(N - 马来酰亚胺甲基)醚阻断的巯基数量是N - 乙基马来酰亚胺的两倍。2. 用[(14)C] - 半胱氨酸标记双 -(N - 马来酰亚胺甲基)醚 - 蛋白质化合物表明,70 - 80%被阻断的巯基通过双功能巯基试剂相互连接。3. 在低反应程度(1.5摩尔巯基/ 10(6)克蛋白质)时,儿茶酚胺外流减少。如果每10(6)克蛋白质中被阻断的巯基超过2摩尔,则无论使用哪种巯基试剂,外流都会增强。4. 如果每10(6)克蛋白质中有2 - 4摩尔巯基被阻断,儿茶酚胺内流的抑制作用随被阻断巯基的比例呈线性增加。5. ATP对儿茶酚胺内流和腺苷三磷酸酶活性的保护作用,对双 -(N - 马来酰亚胺甲基)醚中毒的效果比对N - 乙基马来酰亚胺中毒的效果稍差。