Soluble oligomeric TCR and antigen presentation to CTL

可溶性寡聚 TCR 和抗原呈递至 CTL

• 批准号: 6745793
• 负责人: Yuri Sykulev
• 金额: $ 20.99万
• 依托单位: THOMAS JEFFERSON UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2004
• 资助国家: 美国
• 起止时间: 2004-09-30 至 2006-08-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/6745793
• 关键词: T cell receptor; antigen presentation; binding sites; cell line; cytotoxic T lymphocyte; gag protein; major histocompatibility complex; peptide analog; protein engineering; protein structure; vaccinia virus

DESCRIPTION (provided by applicant): It is becoming increasingly evident that along with the level of cognate peptide-MHC complexes (pMHC) their distribution on the cell surface as well as association with other membrane proteins also influences the antigen presentation. We have shown that MHC class I molecules (MHC-I) are co-clustered with adhesion molecules (ICAM-1) in both membrane rafts and soluble membrane fraction and that productive engagement of these molecules leads to their additional recruitment into rafts and increased association with Scr kinases. Disruption of the raft integrity on target cells decreases potency of viral peptides presentation to CTL. We believe that productive engagement of raft-included MHC-I and ICAM-1 during CTL-target cell encounter results in a signaling that augment presentation of cognate pMHC complexes by target cells to CTL. Based on this, we are set up to investigate functional significance of molecular assemblies on target cells and CTL. We want to identify membrane and intracellular proteins involving in these assemblies and to define mechanisms of "cross-talk" between these molecules. Our efforts are supported by 5 RO1 AI52812-01 Grant from NIAID. One important aspect of the proposal has been missing thus far. Namely, it is essential to determine the level and distribution of cognate pMHC complexes on target cells. This requires a reagent that can distinguish MHC molecules loaded with a peptide of interest from other pMHC complexes. A soluble TCR analog specific for a given pMHC may serve as an elegant tool to probe the pMHC on the surface of target cells. Because of the relatively low affinity of the TCR-pMHC reaction, soluble TCR should be oligomerized to increase the avidity of the binding. We have shown that tetrameric TCR from CTL clone D3 specific for p17 Gag epitope SLYNTVATL (SL9) can specifically detect the presence of SL9-HLA-A2 complexes on target cells. However, at lower epitope density the distance between the pMHC complexes on the cell surface may be too long for the tetramer to engage all binding sites at the same time resulting in a loss of its avidity. With this in mind, we propose here to produce other forms of oligomeric D3 TCR by increasing the valency of the tetramer and/or the distance between tetramer binding sites. We will use these reagents to characterize the distribution of SL9-HLA-A2 complexes on target cells infected with recombinant Vaccinia virus carrying HIV Gag and will determine how this parameter influences sensitivity and magnitude of CTL responses. In the future, these new reagents will be used to detect HIV infected cells in samples derived from infected individuals.

描述（由申请人提供）：越来越明显的是，随着同源肽- mhc复合物（pMHC）的水平，它们在细胞表面的分布以及与其他膜蛋白的结合也会影响抗原呈递。我们已经证明MHC I类分子（MHC-I）在膜筏和可溶性膜组分中与粘附分子（ICAM-1）共簇，这些分子的有效结合导致它们额外被募集到膜筏中，并增加与Scr激酶的关联。破坏靶细胞上的筏完整性会降低病毒肽向CTL呈递的效力。我们认为，在CTL靶细胞遭遇过程中，筏包涵的mhc -1和ICAM-1的有效参与导致信号传导，增强了靶细胞对CTL的同源pMHC复合物的呈递。在此基础上，我们将探讨分子组装对靶细胞和CTL的功能意义。我们希望鉴定参与这些组装的膜和细胞内蛋白质，并确定这些分子之间的“串扰”机制。我们的工作得到了NIAID的5 RO1 AI52812-01补助金的支持。到目前为止，该提案的一个重要方面一直被忽视。也就是说，确定同源pMHC复合物在靶细胞上的水平和分布是至关重要的。这需要一种试剂，可以区分MHC分子装载的目的肽从其他pMHC复合物。针对特定pMHC的可溶性TCR模拟物可以作为探测靶细胞表面pMHC的优雅工具。由于TCR- pmhc反应的亲和力相对较低，因此应将可溶性TCR寡聚化以增加结合的亲切度。我们已经证明，来自CTL克隆D3特异性p17 Gag表位SLYNTVATL （SL9）的四聚体TCR可以特异性检测靶细胞上SL9- hla - a2复合物的存在。然而，在较低的表位密度下，细胞表面上pMHC复合物之间的距离可能太长，使得四聚体无法同时结合所有结合位点，从而导致其亲和性丧失。考虑到这一点，我们建议通过增加四聚体的价和/或四聚体结合位点之间的距离来生产其他形式的低聚D3 TCR。我们将使用这些试剂来表征SL9-HLA-A2复合物在携带HIV Gag的重组痘苗病毒感染的靶细胞上的分布，并将确定该参数如何影响CTL反应的敏感性和强度。未来，这些新试剂将用于检测来自受感染个体的HIV感染细胞样本。