Section of Pulmonary/Critical Care, Center for Nanomedicine, Department of Medicine, University of Chicago, Chicago, Illinois 60637, USA.
J Biol Chem. 2011 Jun 24;286(25):22139-46. doi: 10.1074/jbc.M111.240002. Epub 2011 May 4.
Atomic force microscopy was used to study the three-dimensional molecular topography and calcium-sensitive conformational changes of Connexin40 hemichannels (connexons) reconstituted in 1,2-dioeloyl-sn-glycero-3-phosphatidylcholine lipid bilayers. Two classes of objects were observed that differed in their protrusion heights above the bilayer (2.6 versus 4.2 nm). Comparison to reconstituted connexons containing Connexin40 truncated to eliminate most of its C-terminal cytoplasmic domain showed that the two height classes corresponded to the shorter extracellular and taller cytoplasmic aspects of the hemichannels and that the C-terminal tail of Connexin40 contributes ∼1.6 nm in thickness. Hemichannels imaged in solutions containing < 10 μm Ca(2+) showed 3.1-3.2 nm depressions (openings) in 30% of the cytoplasmic faces and 65% of the extracellular faces, and high-resolution three-dimensional topography of extracellular or cytoplasmic aspects of some connexons was observed. After addition of 3.6 mm Ca(2+), > 75% of the connexons in either orientation adopted closed conformations. In contrast, hemichannels imaged in the presence of 0.1 mm EDTA showed large (5.6- to 5.8-nm diameter) openings in nearly all hemichannels regardless of orientation, and detailed topography was visible in many connexons. Real-time imaging following the addition of 3.6 mm Ca(2+) showed transitions of both extracellular and cytoplasmic orientations from "open" into "closed" conformations within several minutes. These studies provide the first high-resolution topographic information regarding a connexin with a large cytoplasmic domain and suggest that the extramembranous portions of Connexin40 contribute to a channel entrance that is relaxed by chelation of residual divalent cations.
原子力显微镜用于研究在 1,2-二油酰基-sn-甘油-3-磷酸胆碱脂质双层中重建的间隙连接蛋白 40 半通道(连接子)的三维分子形貌和钙敏感性构象变化。观察到两类物体,它们在双层上方的突出高度不同(2.6 与 4.2nm)。与含有截断大部分 C 末端胞质域的间隙连接蛋白 40 的重建连接子进行比较表明,这两个高度类对应于半通道的较短细胞外和较高的细胞质方面,并且间隙连接蛋白 40 的 C 末端尾巴贡献了约 1.6nm 的厚度。在含有 <10μmCa2+的溶液中成像的半通道显示细胞质面的 30%和细胞外面的 65%有 3.1-3.2nm 的凹陷(开口),并且观察到一些连接子的细胞外或细胞质方面的高分辨率三维形貌。加入 3.6mmCa2+后,无论是哪种取向,超过 75%的连接子都采用封闭构象。相比之下,在存在 0.1mmEDTA 的情况下成像的半通道显示出几乎所有半通道中都有大(5.6-至 5.8nm 直径)开口,并且许多连接子中可见详细的形貌。在加入 3.6mmCa2+后进行实时成像显示,几分钟内,无论是细胞外还是细胞质取向的连接子都从“开放”状态转变为“关闭”状态。这些研究提供了第一个关于具有大胞质域的连接蛋白的高分辨率形貌信息,并表明间隙连接蛋白 40 的跨膜部分有助于通道入口,该入口通过螯合残留的二价阳离子而松弛。