Department of Molecular and Cell Biology, University of California Berkeley, Berkeley CA 94720, USA; California Institute for Quantitative Biosciences, University of California, Berkeley, CA, 94720, USA.
Department of Molecular and Cell Biology, University of California Berkeley, Berkeley CA 94720, USA; California Institute for Quantitative Biosciences, University of California, Berkeley, CA, 94720, USA; Helen Wills Neuroscience Institute, University of California, Berkeley, CA 94720, USA.
Curr Opin Struct Biol. 2023 Apr;79:102544. doi: 10.1016/j.sbi.2023.102544. Epub 2023 Feb 16.
Amino acid pools in the cell are monitored by dedicated sensors, whose structures are now coming into view. The lysosomal Rag GTPases are central to this pathway, and the regulation of their GAP complexes, FLCN-FNIP and GATOR1, have been worked out in detail. For FLCN-FNIP, the entire chain of events from the arginine transporter SLC38A9 to substrate-specific mTORC1 activation has been visualized. The structure GATOR2 has been determined, hinting at an ordering of amino acid signaling across a larger size scale than anticipated. The centerpiece of lysosomal signaling, mTORC1, has been revealed to recognize its substrates by more nuanced and substrate-specific mechanisms than previous appreciated. Beyond the well-studied Rag GTPase and mTORC1 machinery, another lysosomal amino acid sensor/effector system, that of PQLC2 and the C9orf72-containing CSW complex, is coming into structural view. These developments hold promise for further insights into lysosomal physiology and lysosome-centric therapeutics.
细胞中的氨基酸池由专门的传感器监测,其结构现在逐渐清晰。溶酶体 Rag GTP 酶是该途径的核心,其 GAP 复合物 FLCN-FNIP 和 GATOR1 的调节已被详细阐明。对于 FLCN-FNIP,从精氨酸转运蛋白 SLC38A9 到底物特异性 mTORC1 激活的整个事件链已经可视化。GATOR2 的结构已经确定,暗示了在比预期更大的规模上跨氨基酸信号传递的顺序。溶酶体信号的核心 mTORC1 已被揭示出通过比以前理解的更细致和底物特异性的机制来识别其底物。除了研究充分的 Rag GTP 酶和 mTORC1 机制外,另一种溶酶体氨基酸传感器/效应器系统,即 PQLC2 和包含 C9orf72 的 CSW 复合物,也正在进入结构视野。这些进展有望进一步深入了解溶酶体生理学和以溶酶体为中心的治疗方法。