Vargas F, Khan S H, Diakun K R
Department of Molecular Immunology, Roswell Park Cancer Institute, New York.
Immunol Invest. 1992 Dec;21(7):671-84. doi: 10.3109/08820139209069403.
The para-aminophenyl derivative of Man alpha 1-->2Man alpha 1-->6Man alpha 1-->was coupled via a diazotization reaction to bovine serum albumin, and the resulting glycoconjugate was used to immunize two rabbits. The resultant antisera were tested for reactivity with a number of related mono, di- and trisaccharides to determine the immunodominant portion of this trisaccharide. Two populations of antibody resulted, one of which required the reducing end mannose, and could react with either an N-acetylglucosamine or a mannose as the penultimate sugar. The other population reacted with the Man alpha 1-->2Man alpha 1-->6Man alpha 1-->. The aglycone moiety and its configurations play an important role in determining the specificity of antibodies to this synthetic antigen. The similarity of this reactivity to the reactivity of mannose binding lectins is discussed.
Manα1→2Manα1→6Manα1→的对氨基苯基衍生物通过重氮化反应与牛血清白蛋白偶联,所得糖缀合物用于免疫两只兔子。检测所得抗血清与多种相关单糖、二糖和三糖的反应性,以确定该三糖的免疫显性部分。产生了两类抗体,其中一类需要还原端甘露糖,并且可以与作为倒数第二个糖的N-乙酰葡糖胺或甘露糖发生反应。另一类抗体与Manα1→2Manα1→6Manα1→发生反应。糖苷配基部分及其构型在决定针对该合成抗原的抗体特异性方面起重要作用。讨论了这种反应性与甘露糖结合凝集素反应性的相似性。