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单克隆抗体识别的细胞毒性T淋巴细胞T200糖蛋白的功能修饰

Functional modifications of cytotoxic T-lymphocyte T200 glycoprotein recognized by monoclonal antibodies.

作者信息

Lefrançois L, Bevan M J

出版信息

Nature. 1985;314(6010):449-52. doi: 10.1038/314449a0.

Abstract

Plasma membrane glycoproteins of cytotoxic T lymphocytes (CTLs) are involved in the binding to and subsequent destruction of appropriate target cells. The electrophoretic profile of surface proteins of mature CTLs, particularly those of high relative molecular mass (Mr), is markedly different from that of naive peripheral T cells or non-cytolytic T cells, suggesting the possible involvement of these molecules in the activation of CTLs and/or in the lytic process itself. By generating monoclonal antibodies to cell-surface proteins of CTL clones, we have now detected CTL-specific modifications in one of these high-Mr membrane proteins, T200. Although forms of T200 are found on a wide variety of cell types, the neoantigenic determinants recognized by our antibodies are present exclusively on activated T cells and in high concentrations only on CTLs. Furthermore, the expression of the modifications recognized by our antibodies is influenced by soluble factors and also seems to have functional significance, as monoclonal antibodies specific for these novel epitopes block cytolytic activity.

摘要

细胞毒性T淋巴细胞(CTL)的质膜糖蛋白参与与合适靶细胞的结合及随后对其的破坏。成熟CTL表面蛋白的电泳图谱,尤其是那些相对分子质量(Mr)高的蛋白,与未致敏外周T细胞或非细胞溶解T细胞的电泳图谱明显不同,这表明这些分子可能参与CTL的激活和/或溶解过程本身。通过产生针对CTL克隆细胞表面蛋白的单克隆抗体,我们现在已经在这些高Mr膜蛋白之一的T200中检测到CTL特异性修饰。尽管在多种细胞类型上都能发现T200的形式,但我们抗体识别的新抗原决定簇仅存在于活化的T细胞上,且仅在CTL中浓度较高。此外,我们抗体识别的修饰的表达受可溶性因子影响,并且似乎也具有功能意义,因为针对这些新表位的单克隆抗体可阻断细胞溶解活性。

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