Gerity E, Conway T P
J Immunol Methods. 1984 Mar 30;68(1-2):131-5. doi: 10.1016/0022-1759(84)90143-1.
Unassociated human beta 2-microglobulin (beta 2m) and histocompatibility peptide associated beta 2-microglobulin produce significantly different inhibition curves in a competitive binding assay with rabbit anti-beta 2-microglobulin. This difference disallows the use of the rabbit antisera for measuring MHC-beta 2-microglobulin complex concentration using free beta 2m as a standard. Presumably the close amino acid sequence homology between human and rabbit beta 2-microglobulin results in rabbit antisera against a small number of epitopes, some of which are covered or conformationally altered in the MHC-beta 2-microglobulin complex. A monoclonal anti-beta 2-microglobulin antibody, LG1 reacted equally well with both forms of beta 2-microglobulin and is used to measure the concentration of beta 2-microglobulin in the histocompatibility peptide complex.
游离的人β2-微球蛋白(β2m)与组织相容性肽相关的β2-微球蛋白在与兔抗β2-微球蛋白的竞争性结合试验中产生显著不同的抑制曲线。这种差异使得无法使用兔抗血清以游离β2m为标准来测量MHC-β2-微球蛋白复合物的浓度。据推测,人和兔β2-微球蛋白之间紧密的氨基酸序列同源性导致兔抗血清针对少数表位,其中一些在MHC-β2-微球蛋白复合物中被覆盖或构象发生改变。一种单克隆抗β2-微球蛋白抗体LG1与两种形式的β2-微球蛋白反应同样良好,可用于测量组织相容性肽复合物中β2-微球蛋白的浓度。