5ZAU
Complex of the human FYN SH3 and monobody binder
5ZAU の概要
| エントリーDOI | 10.2210/pdb5zau/pdb |
| 分子名称 | Tyrosine-protein kinase Fyn, Monobody Binder (2 entities in total) |
| 機能のキーワード | complex, signaling protein |
| 由来する生物種 | Homo sapiens (Human) 詳細 |
| タンパク質・核酸の鎖数 | 2 |
| 化学式量合計 | 13894.74 |
| 構造登録者 | |
| 主引用文献 | Mukherjee, A.,Singh, R.,Udayan, S.,Biswas, S.,Reddy, P.P.,Manmadhan, S.,George, G.,Kumar, S.,Das, R.,Rao, B.M.,Gulyani, A. A Fyn biosensor reveals pulsatile, spatially localized kinase activity and signaling crosstalk in live mammalian cells. Elife, 9:-, 2020 Cited by PubMed Abstract: Cell behavior is controlled through spatio-temporally localized protein activity. Despite unique and often contradictory roles played by Src-family-kinases (SFKs) in regulating cell physiology, activity patterns of individual SFKs have remained elusive. Here, we report a biosensor for specifically visualizing active conformation of SFK-Fyn in live cells. We deployed combinatorial library screening to isolate a binding-protein (F29) targeting activated Fyn. Nuclear-magnetic-resonance (NMR) analysis provides the structural basis of F29 specificity for Fyn over homologous SFKs. Using F29, we engineered a sensitive, minimally-perturbing fluorescence-resonance-energy-transfer (FRET) biosensor () that reveals cellular Fyn activity to be spatially localized, pulsatile and sensitive to adhesion/integrin signaling. Strikingly, growth factor stimulation further enhanced Fyn activity in pre-activated intracellular zones. However, inhibition of focal-adhesion-kinase activity not only attenuates Fyn activity, but abolishes growth-factor modulation. imaging uncovers spatially organized, sensitized signaling clusters, direct crosstalk between integrin and growth-factor-signaling, and clarifies how compartmentalized Src-kinase activity may drive cell fate. PubMed: 32017701DOI: 10.7554/eLife.50571 主引用文献が同じPDBエントリー |
| 実験手法 | SOLUTION NMR |
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