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10.1038/cr.2017.42

http://scihub22266oqcxt.onion/10.1038/cr.2017.42
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C5385618!5385618!28337984
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suck abstract from ncbi


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pmid28337984      Cell+Res 2017 ; 27 (4): 505-25
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  • Lipid-dependent conformational dynamics underlie the functional versatility of T-cell receptor #MMPMID28337984
  • Guo X; Yan C; Li H; Huang W; Shi X; Huang M; Wang Y; Pan W; Cai M; Li L; Wu W; Bai Y; Zhang C; Liu Z; Wang X; Zhang XF; Tang C; Wang H; Liu W; Ouyang B; Wong CC; Cao Y; Xu C
  • Cell Res 2017[Apr]; 27 (4): 505-25 PMID28337984show ga
  • T-cell receptor-CD3 complex (TCR) is a versatile signaling machine that can initiate antigen-specific immune responses based on various biochemical changes of CD3 cytoplasmic domains, but the underlying structural basis remains elusive. Here we developed biophysical approaches to study the conformational dynamics of CD3? cytoplasmic domain (CD3?CD). At the single-molecule level, we found that CD3?CD could have multiple conformational states with different openness of three functional motifs, i.e., ITAM, BRS and PRS. These conformations were generated because different regions of CD3?CD had heterogeneous lipid-binding properties and therefore had heterogeneous dynamics. Live-cell imaging experiments demonstrated that different antigen stimulations could stabilize CD3?CD at different conformations. Lipid-dependent conformational dynamics thus provide structural basis for the versatile signaling property of TCR.
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