Pichla S L, Murali R, Burnett R M
Wistar Institute, Philadelphia, Pennsylvania 19104, USA.
J Struct Biol. 1997 Jun;119(1):6-16. doi: 10.1006/jsbi.1997.3857.
The GD2 ganglioside is a cell-surface component that appears on the surface of metastatic melanoma cells and is a marker for the progression of the disease. The ME36.1 monoclonal antibody binds to the GD2 ganglioside and has shown potential as a therapeutic antibody. ME36.1 is a possible alternative therapy to radiation, which is often ineffective in late-stage melanoma. The crystal structure of the Fab fragment of ME36.1 has been determined using molecular replacement and refined to an R factor of 20.4% at 2.8 A resolution. The model has good geometry with root-mean-square deviations of 0.008 A from ideal bond lengths and 1.7 degrees from ideal bond angles. The crystal structure of the ME36.1 Fab shows that its complementarity determining region forms a groove-shaped binding site rather than the pocket-type observed in other sugar binding Fabs. Molecular modeling has placed a four-residue sugar, representative of GD2, in the antigen binding site. The GD2 sugar moiety is stabilized by a network of hydrogen bonds that define the specificity of ME36.1 toward its antigen.
GD2神经节苷脂是一种细胞表面成分,出现在转移性黑色素瘤细胞表面,是该疾病进展的标志物。ME36.1单克隆抗体与GD2神经节苷脂结合,已显示出作为治疗性抗体的潜力。ME36.1是放疗的一种可能替代疗法,放疗在晚期黑色素瘤中往往无效。ME36.1的Fab片段的晶体结构已通过分子置换确定,并在2.8埃分辨率下精修至R因子为20.4%。该模型具有良好的几何结构,与理想键长的均方根偏差为0.008埃,与理想键角的偏差为1.7度。ME36.1 Fab的晶体结构表明,其互补决定区形成一个槽形结合位点,而不是其他糖结合Fab中观察到的口袋型。分子模拟已将代表GD2的四残基糖置于抗原结合位点。GD2糖部分通过氢键网络稳定,这些氢键定义了ME36.1对其抗原的特异性。