Miller K R, Staehelin L A
J Cell Biol. 1976 Jan;68(1):30-47. doi: 10.1083/jcb.68.1.30.
The structure of the spinach thylakoid outer surface has been examined by deepetching, a technique which exposes the true surfaces of biological membranes by sublimination of frozen dilute buffer. The membrane surface is covered with large (150 A average diameter) and small (90 A average diameter) particles. Approximately 30% of the large particles can be removed under conditions reported to selectively remove carboxydismutase from the membrane surface. The remaining large particles can be removed only under conditions which cause a loss of coupling factor activity. When purified coupling factor is readded to membranes from which all coupling factor activity has been removed, large particles reappear, indicating that they represent coupling factor molecules. Since the number of particles and the amount of ATPase activity in the reconstituted and control membranes were the same, coupling factor molecules may be attached to specific binding sites. Analysis of antibody labeling experiments, enzyme assays, and experiments involving the unstacking and restacking of thylakoid membranes indicate that coupling factor is excluded from regions of membrane stacking (grana) and is present only in unstacked membrane regions. The exclusion of coupling factor from grana, which are known to be centers of intense photosynthetic activity, strongly suggests that the mechanism coupling electron transport to photophosphorylation is indirect. In addition to the large and small particles, in some cases regularly spaced ridges are visible on the outer surface after unstacking. Coupling factor binding sites seem to be excluded from regions where these structures occur.
通过深度蚀刻技术研究了菠菜类囊体外表面的结构,该技术通过冷冻稀缓冲液的升华来暴露生物膜的真实表面。膜表面覆盖着大颗粒(平均直径150埃)和小颗粒(平均直径90埃)。在据报道能从膜表面选择性去除羧化歧化酶的条件下,约30%的大颗粒可以被去除。其余的大颗粒只有在导致偶联因子活性丧失的条件下才能被去除。当将纯化的偶联因子重新添加到所有偶联因子活性都已被去除的膜中时,大颗粒重新出现,表明它们代表偶联因子分子。由于重构膜和对照膜中的颗粒数量以及ATP酶活性相同,偶联因子分子可能附着在特定的结合位点上。抗体标记实验、酶分析以及涉及类囊体膜解堆叠和重新堆叠的实验分析表明,偶联因子被排除在膜堆叠区域(基粒)之外,仅存在于未堆叠的膜区域。已知基粒是强烈光合活性的中心,偶联因子被排除在基粒之外,这强烈表明将电子传递与光合磷酸化偶联的机制是间接的。除了大颗粒和小颗粒外,在某些情况下,解堆叠后在外表面可见规则间隔的脊。偶联因子结合位点似乎被排除在这些结构出现的区域之外。