Laboratory of Molecular Biology, Cambridge, UK.
Autophagy. 2021 Mar;17(3):823-825. doi: 10.1080/15548627.2021.1872190. Epub 2021 Jan 15.
Phosphatidylinositol-3-phosphate (PtdIns3P) is essential for generating autophagosomes and regulating endocytic trafficking. Recently, we have shown that the activities of human PIK3C3/VPS34-containing complexes I and II, which synthesize PtdIns3P, are greatly affected by three membrane physicochemical parameters: lipid unsaturation, membrane curvature, and negative charge. Both complexes are more active on membranes composed of unsaturated lipids than saturated lipids, and high membrane curvature can compensate for the negative effect of high lipid saturation. Negatively charged phosphatidylserine (PS) activates the complexes, as well as PIK3C3/VPS34 alone. The kinase activity of complex I depends critically on the ATG14 BATS domain, whereas complex II relies on the BECN1 BARA domain. Our findings highlight the importance of the membrane character as sensed by the unique membrane binding motifs/domain of the complexes for regulating PIK3C3/VPS34 activity.
磷脂酰肌醇-3-磷酸 (PtdIns3P) 对于生成自噬体和调节内吞运输至关重要。最近,我们已经表明,合成 PtdIns3P 的人类 PIK3C3/VPS34 包含复合物 I 和 II 的活性受到三个膜物理化学参数的极大影响:脂质不饱和、膜曲率和负电荷。两个复合物在由不饱和脂质组成的膜上比在饱和脂质组成的膜上更活跃,而高曲率的膜可以弥补高脂质饱和度的负面影响。带负电荷的磷脂酰丝氨酸 (PS) 可激活复合物,以及单独的 PIK3C3/VPS34。复合物 I 的激酶活性严重依赖于 ATG14 BATS 结构域,而复合物 II 则依赖于 BECN1 BARA 结构域。我们的发现强调了复合物独特的膜结合基序/结构域感知膜特性对于调节 PIK3C3/VPS34 活性的重要性。