Suh W K, Mitchell E K, Yang Y, Peterson P A, Waneck G L, Williams D B
Department of Biochemistry, University of Toronto, Ontario, Canada.
J Exp Med. 1996 Aug 1;184(2):337-48. doi: 10.1084/jem.184.2.337.
Newly assembled heavy chain-beta 2m heterodimers of class I histocompatibility molecules associate with the endoplasmic reticulum (ER) peptide transporter, TAP, and subsequently dissociate from TAP in parallel with their transport from the ER to the Golgi apparatus. It appears that TAP-associated class I molecules are waiting to bind appropriate peptides before they dissociate from TAP and leave the ER since binding of high affinity peptides to class I molecules in vitro leads to dissociation of TAP-class I complexes. In further support of this notion, we report that limiting peptide supply through inhibition of proteasome activities prolongs the association of mouse class I molecules with TAP and concomitantly slows their transport to the Golgi apparatus. By using a series of deletion mutants and hybrid class I molecules we demonstrate that the extracellular domains of class I molecules are sufficient for their peptide-regulated interaction with TAP. Furthermore, based on the inability of an alpha 3 domain-specific mAb to recognize TAP-class I complexes and the fact that a point mutant of the Dd molecule at residue 222 is unable to bind to TAP, it is likely that a major site of interaction with TAP resides in the membrane-proximal region of the heavy chain alpha 3 domain. Finally, we examined the relationship between the interaction of mouse heavy chain-beta 2m heterodimers with TAP and with the resident ER chaperone, calnexin. Most heterodimers that bound to TAP were found to associate simultaneously with calnexin. Upon delivery of peptide to class I molecules in permeabilized cells, dissociation from TAP was observed but the interaction with calnexin was largely maintained. Therefore, both TAP and calnexin may participate in the ER retention of peptide-deficient class I molecules. However, since release from calnexin occurs after dissociation from TAP, it appears that calnexin ultimately determines if a class I molecule is to be exported from the ER.
新组装的I类组织相容性分子重链-β2m异二聚体与内质网(ER)肽转运体TAP结合,随后随着它们从内质网转运到高尔基体而与TAP解离。似乎与TAP相关的I类分子在从TAP解离并离开内质网之前,正等待结合合适的肽,因为在体外高亲和力肽与I类分子的结合会导致TAP-I类复合物的解离。为进一步支持这一观点,我们报道通过抑制蛋白酶体活性来限制肽供应,会延长小鼠I类分子与TAP的结合,并同时减缓它们向高尔基体的转运。通过使用一系列缺失突变体和杂交I类分子,我们证明I类分子的细胞外结构域足以实现其与TAP的肽调节相互作用。此外,基于α3结构域特异性单克隆抗体无法识别TAP-I类复合物,以及Dd分子在第222位残基处的点突变体无法与TAP结合这一事实,与TAP相互作用的主要位点可能位于重链α3结构域的膜近端区域。最后,我们研究了小鼠重链-β2m异二聚体与TAP以及与内质网驻留伴侣钙连蛋白之间相互作用的关系。发现大多数与TAP结合的异二聚体同时也与钙连蛋白结合。在通透细胞中将肽递送至I类分子后,观察到与TAP的解离,但与钙连蛋白的相互作用在很大程度上得以维持。因此,TAP和钙连蛋白可能都参与了缺乏肽的I类分子在内质网中的滞留。然而,由于从钙连蛋白上的释放发生在从TAP解离之后,似乎钙连蛋白最终决定了I类分子是否要从内质网输出。