Hamburger R N, Douglass J H
Immunology. 1969 Oct;17(4):587-91.
Using the classical hapten inhibition technique, antibody binding sites on the chloramphenicol molecule were explored. Sixteen compounds related to chloramphenicol, but with varying degrees of change in their structure, were examined for inhibiting ability at 1-, 10- and 100-μg levels. The removal of the two chlorine atoms accounted for the greatest loss of antibody binding capacity. The major antigenic sites are separate from the sites critical for the antibiotic activity of chloramphenicol.
采用经典的半抗原抑制技术,对氯霉素分子上的抗体结合位点进行了探究。研究了16种与氯霉素相关但结构有不同程度变化的化合物在1微克、10微克和100微克水平下的抑制能力。去除两个氯原子导致抗体结合能力丧失最多。主要抗原位点与氯霉素抗生素活性的关键位点是分开的。