Gillies Laura A, Du Han, Peters Bjoern, Knudson C Michael, Newmeyer Donald D, Kuwana Tomomi
La Jolla Institute, La Jolla, CA 92037.
Department of Pathology, University of Iowa, Iowa City, IA 52242.
Mol Biol Cell. 2015 Jan 15;26(2):339-49. doi: 10.1091/mbc.E13-11-0638. Epub 2014 Nov 19.
Bax induces mitochondrial outer membrane permeabilization (MOMP), a critical step in apoptosis in which proteins are released into the cytoplasm. To resolve aspects of the mechanism, we used cryo-electron microscopy (cryo-EM) to visualize Bax-induced pores in purified mitochondrial outer membranes (MOMs). We observed solitary pores that exhibited negative curvature at their edges. Over time, the pores grew to ∼ 100-160 nm in diameter after 60-90 min, with some pores measuring more than 300 nm. We confirmed these results using flow cytometry, which we used to monitor the release of fluorescent dextrans from isolated MOM vesicles. The dextran molecules were released gradually, in a manner constrained by pore size. However, the release rates were consistent over a range of dextran sizes (10-500 kDa). We concluded that the pores were not static but widened dramatically to release molecules of different sizes. Taken together, the data from cryo-EM and flow cytometry argue that Bax promotes MOMP by inducing the formation of large, growing pores through a mechanism involving membrane-curvature stress.
Bax诱导线粒体外膜通透性改变(MOMP),这是细胞凋亡中的关键步骤,在此过程中蛋白质释放到细胞质中。为了阐明该机制的各个方面,我们使用冷冻电子显微镜(cryo-EM)观察纯化的线粒体外膜(MOMs)中Bax诱导形成的孔。我们观察到单个孔在其边缘呈现负曲率。随着时间的推移,60 - 90分钟后孔直径增长到约100 - 160纳米,有些孔尺寸超过300纳米。我们使用流式细胞术证实了这些结果,该技术用于监测从分离的MOM囊泡中荧光葡聚糖的释放。葡聚糖分子以受孔径限制的方式逐渐释放。然而,在一系列葡聚糖大小(10 - 500 kDa)范围内释放速率是一致的。我们得出结论,这些孔不是静态的,而是会显著扩大以释放不同大小的分子。综合来看,冷冻电子显微镜和流式细胞术的数据表明,Bax通过涉及膜曲率应力的机制诱导形成大的、不断增大的孔来促进MOMP。