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间隙连接的生物物理学

Biophysics of gap junctions.

作者信息

Bennett M V, Verselis V K

机构信息

Department of Neuroscience, Albert Einstein College of Medicine, Bronx, NY 10461.

出版信息

Semin Cell Biol. 1992 Feb;3(1):29-47. doi: 10.1016/s1043-4682(10)80006-6.

Abstract

Gap junction channels, now known to be formed of connexins, connect the interiors of apposed cells. These channels can be opened and closed by various physiological stimuli and experimental treatments. They are permeable to ions and neutral molecules up to a size of about 1 kDa or 1.5 nm diameter, including second messengers and metabolites. The processes of gating and of permeation are the subject of this review. Voltage is a readily applied stimulus, and transjunctional voltages, or those between cytoplasm and exterior, affect most junctions. Single channel transitions between open and closed states are rapid and presumably involve a charge movement as occurs with channels of electrically excitable channels of nerve and muscle. Identification of gating domains and charges by domain replacement and site-directed mutagenesis is being pursued. Raising cytoplasmic H+ or Ca2+ concentrations rapidly reduces junctional conductance, and this action is generally reversible, at least in part. A number of lipophilic alcohols, fatty acids and volatile anesthetics have similar actions. Phosphorylation also modulates junctional conductance, and in several cases, sites of phosphorylation are known. These gating processes appear similar to those induced by voltage. Permeability measurement indicates that the channel is aqueous and that permeation is by diffusion with only minor interactions with the channel wall. Differences among junctions are known, but further characterization of connexin and cell specificity is required.

摘要

间隙连接通道现在已知是由连接蛋白构成的,它连接相邻细胞的内部。这些通道可以通过各种生理刺激和实验处理来打开和关闭。它们对离子和直径约为1 kDa或1.5 nm大小的中性分子具有通透性,包括第二信使和代谢产物。通道的门控和通透过程是本综述的主题。电压是一种易于施加的刺激,跨连接电压,即细胞质与外部之间的电压,会影响大多数连接。通道在开放和关闭状态之间的单通道转换很快,大概涉及电荷移动,就像神经和肌肉的电兴奋性通道那样。正在通过结构域替换和定点诱变来鉴定门控结构域和电荷。提高细胞质中的H⁺或Ca²⁺浓度会迅速降低连接电导,并且这种作用通常至少部分是可逆的。许多亲脂性醇、脂肪酸和挥发性麻醉剂也有类似作用。磷酸化也会调节连接电导,在一些情况下,磷酸化位点是已知的。这些门控过程似乎与电压诱导的过程相似。通透性测量表明通道是水性的,通透是通过扩散进行的,与通道壁只有轻微的相互作用。不同连接之间的差异是已知的,但还需要进一步表征连接蛋白和细胞特异性。

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