...
首页> 外文期刊>Infection and immunity >Compartmentalization of defined epitopes expressed in Escherichia coli has only a minor influence on efficiency of phagocytic processing for presentation by class I and class II major histocompatibility complex molecules to T cells.
【24h】

Compartmentalization of defined epitopes expressed in Escherichia coli has only a minor influence on efficiency of phagocytic processing for presentation by class I and class II major histocompatibility complex molecules to T cells.

机译:在大肠埃希菌中表达的确定表位的区室化对吞噬加工效率的影响很小,以将I类和II类主要组织相容性复合物分子呈递给T细胞。

获取原文
           

摘要

The effect of abundance and compartmentalization of antigenic epitopes expressed in Escherichia coli on phagocytic processing was studied by expressing fusion proteins containing the epitope from positions 52 to 61 of hen egg white lysozyme [HEL(52-61)], which binds the I-Ak murine major histocompatibility complex class II (MHC-II) molecule or the epitope from positions 257 to 264 of chicken egg ovalbumin [OVA(257-264]), which binds the Kb murine MHC-I molecule. Epitopes expressed as fusion proteins in the outer membrane protein LamB allowed exposure of the epitopes either at the bacterial surface, in the periplasmic space, or in the cytoplasm. Regardless of epitope compartmentalization within the bacterium, MHC-II-restricted or MHC-I-restricted presentation to T hybridoma cells occurred after macrophages phagocytosed bacteria producing the HEL(52-61) epitope or the OVA(257-264) epitope, respectively. Increased epitope abundance within a given microbial compartment resulted in increased processing and presentation to epitope-specific T hybridoma cells. Minor differences in the efficiency of epitope processing between the constructs was observed, and the HEL or OVA epitope exposed in the periplasmic space was processed most efficiently compared with the surface- or cytoplasm-localized epitopes. These differences could be overcome by increasing the amount of epitope per bacterium as little as two to five times. The minor differences in processing efficiency may be due to differing protein contexts of the epitope as well as differing epitope compartmentalizations within the bacteria. Thus, production of abundant epitope is the important parameter influencing processing of epitopes expressed in E. coli to induce T-cell responses rather than targeting of an epitope to a specific bacterial compartment.
机译:通过表达包含蛋清溶菌酶[HEL(52-61)] 52-61位结合I-Ak的抗原决定簇的融合蛋白,研究了大肠杆菌表达的抗原决定簇的丰度和分隔对吞噬过程的影响。鼠类主要组织相容性复合体II类(MHC-II)分子或鸡蛋卵清蛋白[OVA(257-264])的257至264位表位,该表位与Kb鼠MHC-1分子结合。在外膜蛋白LamB中表达为融合蛋白的表位允许表位在细菌表面,周质空间或细胞质中暴露。无论细菌内的表位区分开如何,在巨噬细胞吞噬细菌分别产生HEL(52-61)表位或OVA(257-264)表位之后,MHC-II限制或MHC-I限制呈递给T杂交瘤细胞。给定微生物区隔中表位丰度的增加导致对表位特异性T杂交瘤细胞的加工和呈递增加。观察到构建体之间表位加工效率的微小差异,与表面或细胞质定位的表位相比,周质空间中暴露的HEL或OVA表位处理效率最高。这些差异可以通过将每种细菌的表位数量增加少两倍至五倍来克服。加工效率的细微差异可能是由于表位的不同蛋白质背景以及细菌内不同的表位区分开。因此,丰富表位的产生是影响在大肠杆菌中表达的表位的加工以诱导T细胞应答而不是将表位靶向特定细菌区室的重要参数。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号