Eigenbrot C, Gonzalez T, Mayeda J, Carter P, Werther W, Hotaling T, Fox J, Kessler J
Department of Protein Engineering, Genentech, Inc., South San Francisco, California 94080-4990.
Proteins. 1994 Jan;18(1):49-62. doi: 10.1002/prot.340180107.
X-ray crystal structures of fragments from two different humanized anti-CD18 antibodies are reported. The Fv fragment of the nonbinding version has been refined in space group C2 with a = 64.2 A, b = 61.3 A, c = 51.8 A, and beta = 99 degrees to an R-value of 18.0% at 1.9 A, and the Fab fragment of the tight-binding version has been refined in space group P3 with a = 101. A and c = 45.5 A to an R-value of 17.8% at 3.0 A resolution. The very large difference in their binding affinity (> 1000-fold) is attributed to large and local structural differences in the C-terminal part of CDR-H2, and from this we conclude there is direct contact between this region and antigen when they combine. X-ray structures of antibody-antigen complexes available in the literature have yet to show this part of CDR-H2 in contact with antigen, despite its hypervariable sequence. Implications of this result for antibody humanization are discussed.
报道了两种不同人源化抗CD18抗体片段的X射线晶体结构。非结合型的Fv片段在空间群C2中进行了精修,a = 64.2 Å,b = 61.3 Å,c = 51.8 Å,β = 99°,在1.9 Å分辨率下R值为18.0%;紧密结合型的Fab片段在空间群P3中进行了精修,a = 101 Å,c = 45.5 Å,在3.0 Å分辨率下R值为17.8%。它们结合亲和力的巨大差异(>1000倍)归因于CDR-H2 C末端部分的大规模局部结构差异,由此我们得出结论,当它们结合时,该区域与抗原之间存在直接接触。尽管CDR-H2的序列具有高变异性,但文献中可用的抗体-抗原复合物的X射线结构尚未显示该部分与抗原接触。讨论了该结果对抗体人源化的影响。