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TCRα链易位至内质网腔并被降解。

Translocation of TCR alpha chains into the lumen of the endoplasmic reticulum and their degradation.

作者信息

Shin J, Lee S, Strominger J L

机构信息

Division of Tumor Virology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA 02115.

出版信息

Science. 1993 Mar 26;259(5103):1901-4. doi: 10.1126/science.8456316.

Abstract

After synthesis, the alpha chain of the T cell antigen receptor (TCR alpha) can form a complex with other TCR chains and move to the cell surface, or TCR alpha can undergo degradation in the endoplasmic reticulum (ER) if it remains unassembled. The mechanism of translocation and degradation in the ER is unclear. It was found that the putative transmembrane region of TCR alpha (alpha tm) was incompetent on its own to act as a transmembrane region. Molecules that contained alpha tm were translocated into the ER lumen and then underwent either rapid degradation or secretion, depending on the sequence of the cytoplasmic domain. A specific signal for ER degradation within alpha tm does not appear to be present.

摘要

合成后,T细胞抗原受体(TCRα)的α链可与其他TCR链形成复合物并移动至细胞表面,或者,如果TCRα未组装,它可在内质网(ER)中发生降解。内质网中的转运和降解机制尚不清楚。研究发现,TCRα假定的跨膜区(αtm)自身不能作为跨膜区发挥作用。含有αtm的分子被转运到内质网腔,然后根据胞质结构域的序列进行快速降解或分泌。αtm内似乎不存在内质网降解的特定信号。

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