Hilzenrat Geva, Pandžić Elvis, Yang Zhengmin, Nieves Daniel J, Goyette Jesse, Rossy Jérémie, Ma Yuanqing, Gaus Katharina
EMBL Australia Node in Single Molecule Science, School of Medical Sciences, University of New South Wales, Sydney, Australia; ARC Centre of Excellence in Advanced Molecular Imaging, University of New South Wales, Sydney, Australia; Commonwealth Scientific and Industry Research Organization (CSIRO), Manufacturing, Clayton, Victoria, Australia.
BioMedical Imaging Facility, Mark Wainwright Analytical Centre, University of New South Wales, Sydney, Australia.
Biophys J. 2020 Mar 24;118(6):1489-1501. doi: 10.1016/j.bpj.2020.01.041. Epub 2020 Feb 11.
T cell receptor phosphorylation by Lck is an essential step in T cell activation. It is known that the conformational states of Lck control enzymatic activity; however, the underlying principles of how Lck finds its substrate over the plasma membrane remain elusive. Here, single-particle tracking is paired with photoactivatable localization microscopy to observe the diffusive modes of Lck in the plasma membrane. Individual Lck molecules switched between free and confined diffusion in both resting and stimulated T cells. Lck mutants locked in the open conformation were more confined than Lck mutants in the closed conformation. Further confinement of kinase-dead versions of Lck suggests that Lck confinement was not caused by phosphorylated substrates. Our data support a model in which confined diffusion of open Lck results in high local phosphorylation rates, and inactive, closed Lck diffuses freely to enable long-range distribution over the plasma membrane.
Lck介导的T细胞受体磷酸化是T细胞激活过程中的关键步骤。已知Lck的构象状态控制着酶活性;然而,Lck如何在质膜上找到其底物的潜在机制仍不清楚。在这里,单粒子追踪与光激活定位显微镜相结合,以观察Lck在质膜中的扩散模式。在静息和激活的T细胞中,单个Lck分子在自由扩散和受限扩散之间切换。锁定在开放构象的Lck突变体比处于封闭构象的Lck突变体受到更多限制。对激酶失活型Lck的进一步限制表明,Lck的限制不是由磷酸化底物引起的。我们的数据支持这样一个模型,即开放型Lck的受限扩散导致高局部磷酸化率,而无活性的封闭型Lck自由扩散,从而在质膜上实现长距离分布。