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Microtubular origin of mitotic spindle form birefringence. Demonstration of the applicability of Wiener's equation.有丝分裂纺锤体双折射的微管起源。维纳方程适用性的证明。
J Cell Biol. 1975 Dec;67(3):501-17. doi: 10.1083/jcb.67.3.501.
2
Spindle birefringence of isolated mitotic apparatus: further evidence for two birefringent spindle components.分离的有丝分裂器的纺锤体双折射:两种双折射纺锤体成分的进一步证据。
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3
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本文引用的文献

1
The mitotic apparatus: isolation by controlled pH.有丝分裂器:通过控制pH值进行分离
J Cell Biol. 1962 Jan;12(1):47-55. doi: 10.1083/jcb.12.1.47.
2
THE MITOTIC APPARATUS. PHYSICAL-CHEMICAL FACTORS CONTROLLING STABILITY.有丝分裂器。控制稳定性的物理化学因素。
J Cell Biol. 1965 Apr;25(1):SUPPL:137-44. doi: 10.1083/jcb.25.1.137.
3
FILAMENT LENGTHS IN STRIATED MUSCLE.横纹肌中的细丝长度
J Cell Biol. 1963 Nov;19(2):369-90. doi: 10.1083/jcb.19.2.369.
4
Birefringence of protein solutions and biological systems. I.蛋白质溶液和生物系统的双折射。I.
Biophys J. 1963 Mar;3(2):127-41. doi: 10.1016/s0006-3495(63)86809-5.
5
Studies on depolarization of light at microscope lens surfaces. II. The simultaneous realization of high resolution and high sensitivity with the polarizing microscope.显微镜透镜表面光的去极化研究。II. 偏振显微镜高分辨率和高灵敏度的同时实现。
J Biophys Biochem Cytol. 1957 Nov 25;3(6):831-8. doi: 10.1083/jcb.3.6.831.
6
Cell motility by labile association of molecules. The nature of mitotic spindle fibers and their role in chromosome movement.通过分子的不稳定结合实现细胞运动。有丝分裂纺锤体纤维的性质及其在染色体移动中的作用。
J Gen Physiol. 1967 Jul;50(6):Suppl:259-92.
7
Ultrastructure and birefringence of the isolated mitotic apparatus of marine eggs.海产卵分离有丝分裂器的超微结构和双折射
J Cell Biol. 1967 Sep;34(3):859-83. doi: 10.1083/jcb.34.3.859.
8
Some aspects of microtubules in spermatocyte meiosis in a crane fly (Nephrotoma suturalis Loew): intranuclear and intrachromosomal microtubules.大蚊(Nephrotoma suturalis Loew)精母细胞减数分裂中微管的某些方面:核内和染色体内微管
C R Trav Lab Carlsberg. 1966;35(19):437-55.
9
Observations on the substructure of flagellar fibres.关于鞭毛纤维亚结构的观察
J Cell Sci. 1966 Sep;1(3):351-62. doi: 10.1242/jcs.1.3.351.
10
Intrinsic birefringence of poly-gamma-benzyl-L-glutamate, a helical polypeptide, and the theory of birefringence.螺旋状多肽聚-γ-苄基-L-谷氨酸的固有双折射及双折射理论
Biophys J. 1965 Jul;5(4):531-52. doi: 10.1016/S0006-3495(65)86733-9.

有丝分裂纺锤体双折射的微管起源。维纳方程适用性的证明。

Microtubular origin of mitotic spindle form birefringence. Demonstration of the applicability of Wiener's equation.

作者信息

Sato H, Ellis G W, Inoué S

出版信息

J Cell Biol. 1975 Dec;67(3):501-17. doi: 10.1083/jcb.67.3.501.

DOI:10.1083/jcb.67.3.501
PMID:1238403
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2111675/
Abstract

Meiosis I metaphase spindles were isolated from oocytes of the sea-star Pisaster ochraceus by a method that produced no detectable net loss in spindle birefringence. Some of the spindles were fixed immediately and embedded and sectioned for electron microscopy. Others were laminated between gelatine pellicles in a perfusion chamber, then fixed and sequentially and reversibly imbibed with a series of media of increasing refractive indices. Electron microscopy showed little else besides microtubules in the isolates, and no other component present could account for the observed form birefringence. An Ambronn plot of the birefringent retardation measured during imbibition was a good least squares fit to a computer generated theoretical curve based on the Bragg-Pippard rederivation of the Wiener curve for form birefringence. The data were best fit by the curve for rodlet index (n1) = 1.512, rodlet volume fraction (f) = 0.0206, and coefficient of intrinsic birefringence = 4.7 X 10(-5). The value obtained for n1 is unequivocal and is virtually as good as the refractometer determinations of imbibing medium index on which it is based. The optically interactive volume of the microtubule subunit, calculated from our electron microscope determination of spindle microtubule distribution (106/mum2), 13 protofilaments per microtubules, an 8 nm repeat distance and our best value for f, is compatible with known subunit dimensions as determined by other means. We also report curves fitted to the results of Ambronn imbibition of Bouin's-fixed Lytechinus spindles and to the Noll and Weber muscle imbibition data.

摘要

通过一种在纺锤体双折射方面未检测到明显净损失的方法,从海星赭色皮海星的卵母细胞中分离出减数分裂I中期纺锤体。一些纺锤体立即固定、包埋并切片用于电子显微镜观察。其他纺锤体则夹在灌注室中的明胶薄膜之间,然后固定,并依次用一系列折射率递增的介质进行可逆浸渗。电子显微镜观察显示,分离物中除微管外几乎没有其他物质,且不存在其他成分能够解释所观察到的形态双折射。浸渗过程中测量的双折射延迟的安布隆图与基于维纳曲线的布拉格 - 皮帕德重新推导得到的形态双折射计算机生成理论曲线非常吻合,是很好的最小二乘法拟合。数据最符合棒状指数(n1) = 1.512、棒状体积分数(f) = 0.0206和固有双折射系数 = 4.7×10⁻⁵的曲线。所获得的n1值明确无误,几乎与基于浸渗介质折射率的折射仪测定值一样好。根据我们对纺锤体微管分布的电子显微镜测定(106/μm²)、每根微管13条原纤维、8nm的重复距离以及我们得到的最佳f值计算出的微管亚基的光学相互作用体积,与通过其他方法确定的已知亚基尺寸相符。我们还报告了拟合布因固定的海胆纺锤体的安布隆浸渗结果以及诺尔和韦伯肌肉浸渗数据的曲线。