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Molecular mechanisms of regulatory T cell -mediated rapid suppression in human conventional T cell signalling monitored by phosphoproteomics

机译:调节T细胞介导的磷蛋白酶监测的人类常规T细胞信号中的调节T细胞的快速抑制的分子机制

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摘要

1. This rst phosphoproteomics study on primary T-cells directly suppressed by Tregs reveals a rapid downregulation of phosphorylation on several proteins. 2. A large group of the 29 signicantly regulated phosphoproteins can be mapped to a functional cluster involving RNA processing. 3. The role of the phosphorylated proteins in Treg suppression will be veried with complementary methods, like siRNA knockdown.
机译:1.该RST磷蛋白质学研究直接被Tregs抑制的初级T细胞揭示了几种蛋白质上磷酸化的快速下调。 2. 29个焦虑受调节的磷酸蛋白可以映射到涉及RNA加工的功能簇。 3.将磷酸化蛋白在Treg抑制中的作用将用互补方法来验证,如siRNA敲低。

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