Hayball John D, Lake Richard A
School of Pharmacy and Medical Sciences, University of South Australia, North Tce, Adelaide, South Australia, Australia.
Mol Cell Biochem. 2005 May;273(1-2):1-9. doi: 10.1007/s11010-005-5281-4.
Analysis of the crystal structure of human class II (HLA-DR1) molecules suggests that the alphabeta heterodimer may be further ordered as a dimer of heterodimers (superdimer), leading to the hypothesis that T cell receptor dimerisation is a mechanism for initiating signaling events preceding T cell activation. The interface between pairs of molecules is stabilised by both salt bridges, polar and hydrophobic interactions. The residues that form the superdimer interface occur in three areas distinct from the antigen-binding groove. They can be defined as follows: region 1, beta-beta contacts in the helix of the beta1 domain; region 2, alpha-alpha contacts near the alpha 1/alpha2 domain junction and region 3; alpha-beta contacts in the alpha2/beta2 domains adjacent to the plasma membrane. To determine whether salt bridges and polar interactions formed within these regions are involved in the immune function of the murine MHC class II molecule, I-A(b), appropriate residues in both the alpha and beta chain were identified and mutated to uncharged alanine. Cell lines transfected with different combinations of mutated alpha and beta chains were generated and tested for MHC class II expression, peptide binding capabilities, and ability to present antigenic peptide to an OVA-specific T cell hybridoma. With the exception of two residues in region 2, the substitutions tested did not modulate MHC class II expression, or peptide binding function. When tested for ability to present peptide to an antigen-specific T cell hybridoma, with the exception of mutations in region 2, the substitutions did not appear to abrogate the ability of I-A(b) to stimulate the T cells. These results suggest that mutation of residues in region 2 of the putative superdimer interface have a gross effect on the ability of I-A(b) to be expressed on the cell surface. However, abrogation of salt bridges in region 1 and 3 do not influence I-A(b) cell surface expression, peptide binding or ability to stimulate antigen-specific T cells.
对人类II类(HLA - DR1)分子晶体结构的分析表明,αβ异二聚体可能进一步有序排列成异二聚体的二聚体(超二聚体),从而引出了这样一种假说,即T细胞受体二聚化是在T细胞活化之前启动信号事件的一种机制。分子对之间的界面通过盐桥、极性和疏水相互作用得以稳定。形成超二聚体界面的残基出现在与抗原结合槽不同的三个区域。它们可定义如下:区域1,β1结构域螺旋中的β - β接触;区域2,α1/α2结构域交界处附近的α - α接触以及区域3;与质膜相邻的α2/β2结构域中的α - β接触。为了确定在这些区域内形成的盐桥和极性相互作用是否参与小鼠MHC II类分子I - A(b)的免疫功能,在α链和β链中鉴定出合适的残基并将其突变为不带电荷的丙氨酸。构建了转染不同组合突变α链和β链的细胞系,并对其进行MHC II类表达、肽结合能力以及将抗原肽呈递给OVA特异性T细胞杂交瘤的能力测试。除区域2中的两个残基外,所测试的替换并未调节MHC II类表达或肽结合功能。当测试将肽呈递给抗原特异性T细胞杂交瘤的能力时,除区域2中的突变外,这些替换似乎并未消除I - A(b)刺激T细胞的能力。这些结果表明,假定的超二聚体界面区域2中残基的突变对I - A(b)在细胞表面表达的能力有重大影响。然而,区域1和3中盐桥的消除并不影响I - A(b)的细胞表面表达、肽结合或刺激抗原特异性T细胞的能力。