Peborde J P, Samain D
Centre de transfert en Biotechnologie et Microbiologie (INSA-UPS), Toulouse, France.
Biochim Biophys Acta. 1990 Feb 26;1033(2):207-9. doi: 10.1016/0304-4165(90)90014-n.
Tritiated lipopolysaccharide (LPS) from E. coli K12 was prepared by coupling [3H]ethanolamine to the LPS core residue ketodeoxyoctonate (KDO) via activation of its carboxylic function with N-hydroxysuccinimide or N-hydroxy-sulfosuccinimide. Specific activities of 1.5 microCi/mg and 9 microCi/mg were obtained, respectively. Experiments comparing the activity of native and derivatized LPS suggested that the preparation of the radiolabelled LPS did not alter the structural properties of E. coli K12 LPS. This probe will be useful for studying the interactions between LPS and proteins.
通过用N-羟基琥珀酰亚胺或N-羟基磺基琥珀酰亚胺激活其羧基官能团,将[3H]乙醇胺与脂多糖核心残基酮脱氧辛酮酸(KDO)偶联,制备了来自大肠杆菌K12的氚标记脂多糖(LPS)。分别获得了1.5微居里/毫克和9微居里/毫克的比活。比较天然LPS和衍生化LPS活性的实验表明,放射性标记LPS的制备不会改变大肠杆菌K12 LPS的结构特性。该探针将有助于研究LPS与蛋白质之间的相互作用。