4.5 Article

T Cell Activation Results in Conformational Changes in the Src Family Kinase Lck to Induce Its Activation

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SCIENCE SIGNALING
卷 6, 期 263, 页码 -

出版社

AMER ASSOC ADVANCEMENT SCIENCE
DOI: 10.1126/scisignal.2003607

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资金

  1. German Research Society (DFG) [SFB854, FOR521]
  2. State of Saxony-Anhalt [FKZ: XN0050KL/0206]
  3. Magdeburg Center for Systems Biology (MaCS)
  4. Federal Ministry of Education and Research (BMBF) [FKZ 13N10077]
  5. Austrian Science Fund through the EUROCORES Euromembrane program [LIPIDPROD I0030]
  6. Erwin Schroedinger scholarship program
  7. Austrian Science Fund (FWF) [I 300] Funding Source: researchfish

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The lymphocyte-specific Src family protein tyrosine kinase p56(Lck) (Lck) is essential for T cell development and activation and, hence, for adaptive immune responses. The mechanism by which Lck activity is directed toward specific substrates in response to T cell receptor (TCR) activation remains elusive. We used fluorescence lifetime imaging microscopy to assess the activation-dependent spatiotemporal changes in the conformation of Lck in live human T cells. Kinetic analysis of the fluorescence lifetime of Lck biosensors enabled the direct visualization of the dynamic local opening of 20% of the total amount of Lck proteins after activation of T cells with antibody against CD3 or by superantigen-loaded antigen-presenting cells. Parallel biochemical analysis of TCR complexes revealed that the conformational changes in Lck correlated with the induction of Lck enzymatic activity. These data show the dynamic, local activation through conformational change of Lck at sites of TCR engagement.

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