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CD2上存在CD58和另一种配体CD59的重叠但不完全相同的结合位点。

Overlapping but nonidentical binding sites on CD2 for CD58 and a second ligand CD59.

作者信息

Hahn W C, Menu E, Bothwell A L, Sims P J, Bierer B E

机构信息

Division of Pediatric Oncology, Dana-Farber Cancer Institute, and Harvard Medical School, Boston, MA.

出版信息

Science. 1992 Jun 26;256(5065):1805-7. doi: 10.1126/science.1377404.

Abstract

The interaction of the T cell glycoprotein CD2 with one ligand, CD58, contributes to T cell function. We have identified CD59, a glycoprotein with complement-inhibitory function, as a second physiological ligand for CD2. Antibodies to CD59 inhibit CD2-dependent T cell activation in murine T cell hybridomas expressing human CD2. In an in vitro binding assay with purified CD58 and CD59, CD2+ cells bind not only immobilized CD58 but also CD59. With two complementary approaches, it was demonstrated that the binding sites on CD2 for CD58 and CD59 are overlapping but nonidentical. These observations suggest that direct interactions between CD2 and both CD58 and CD59 contribute to T cell activation and adhesion.

摘要

T细胞糖蛋白CD2与一种配体CD58的相互作用有助于T细胞功能。我们已鉴定出具有补体抑制功能的糖蛋白CD59是CD2的第二种生理配体。针对CD59的抗体可抑制表达人CD2的鼠T细胞杂交瘤中CD2依赖性T细胞活化。在与纯化的CD58和CD59进行的体外结合试验中,CD2 +细胞不仅能结合固定化的CD58,还能结合CD59。通过两种互补方法证明,CD2上CD58和CD59的结合位点重叠但不相同。这些观察结果表明,CD2与CD58和CD59之间的直接相互作用有助于T细胞活化和黏附。

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