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对骨骼肌肌小节 SHG 强度模式的超分子中心对称效应的建模。

Modeling of supramolecular centrosymmetry effect on sarcomeric SHG intensity pattern of skeletal muscles.

机构信息

Institut de Physique de Rennes, UMR UR1-Centre National de la Recherche Scientifique 6251, Rennes, France.

出版信息

Biophys J. 2011 Jul 20;101(2):494-503. doi: 10.1016/j.bpj.2011.05.065.

Abstract

A theoretical far-field second harmonic generation (SHG) imaging radiation pattern is calculated for muscular myosin taking into account both Gouy effect and light diffraction under high focusing excitation. Theoretical analysis, in agreement with experimental results obtained on healthy Xenopus muscles, shows that the increase on intensity at the middle of the sarcomeric SHG intensity pattern is generated by an off-axis constructive interference related to the specific antipolar distribution of myosin molecules within the sarcomere. The best fit of the experimental sarcomeric SHG intensity pattern was obtained with an estimated size of antiparallel, intrathick filaments' packing-width of 115 ± 25 nm localized at the M-band. During proteolysis, experimental sarcomeric SHG intensity pattern exhibits decrease on intensity at the center of the sarcomere. An effective intra- and interthick filaments centrosymmetry of 320 ± 25 nm, in agreement with ultrastructural disorganization observed at the electron microscopy level, was necessary to fit the experimental sarcomeric SHG intensity pattern. Our results show that sarcomeric SHG intensity pattern is very sensitive to misalignment of thick filaments and highlights the potential usefulness of SHG microscopy to diagnose proteolysis-induced muscular disorders.

摘要

考虑到高聚焦激发下的古斯效应和光衍射,我们计算了肌球蛋白的理论远场二次谐波产生(SHG)成像辐射模式。理论分析与在健康的非洲爪蟾肌肉上获得的实验结果一致,表明在肌节 SHG 强度模式的中间强度增加是由与肌球蛋白分子在肌节内的特定反平行分布有关的离轴建设性干涉产生的。通过估计位于 M 带的 115±25nm 长的平行、厚丝包装宽度,对实验肌节 SHG 强度模式进行了最佳拟合。在蛋白酶解过程中,实验肌节 SHG 强度模式在肌节中心的强度降低。为了拟合实验肌节 SHG 强度模式,需要厚丝的有效内和外对称性为 320±25nm,这与在电子显微镜水平观察到的超微结构紊乱一致。我们的结果表明,肌节 SHG 强度模式对厚丝的不对准非常敏感,并突出了 SHG 显微镜在诊断蛋白酶解诱导的肌肉疾病方面的潜在用途。

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