Hao Yudong, Bernstein Sanford I, Pollack Gerald H
Department of Bioengineering, University of Washington, Seattle, Washington 98195, USA.
J Muscle Res Cell Motil. 2004;25(4-5):359-66. doi: 10.1007/s10974-004-0684-5.
As the smallest muscle-cell substructure that retains the intact contractile apparatus, the single myofibril is considered the optimal specimen for muscle mechanics, although its small size also poses some technical difficulties. Myofibrils from Drosophila indirect flight muscle (IFM) are particularly difficult to study because their high passive stiffness makes them hard to handle, and too resistant to stretch to produce enough elongation for the accurate measurement of sarcomere length change. In this study, we devised a novel method for accurate stiffness measurement of single relaxed myofibrils using microfabricated cantilevers and phase contrast microscopy. A special experimental protocol was developed to minimize errors, and some data analysis strategies were used to identify and exclude spurious data. Remarkably consistent results were obtained from Drosophila IFM myofibrils. This novel, high accuracy method is potentially an effective tool for detecting small passive stiffness change in muscle mutants.
作为保留完整收缩装置的最小肌肉细胞亚结构,单个肌原纤维被认为是研究肌肉力学的最佳标本,尽管其尺寸小也带来了一些技术难题。果蝇间接飞行肌(IFM)的肌原纤维特别难以研究,因为其高被动刚度使其难以处理,并且对拉伸的抵抗力太大,无法产生足够的伸长以准确测量肌节长度变化。在本研究中,我们设计了一种使用微加工悬臂和相差显微镜精确测量单个松弛肌原纤维刚度的新方法。制定了特殊的实验方案以尽量减少误差,并使用了一些数据分析策略来识别和排除虚假数据。从果蝇IFM肌原纤维获得了非常一致的结果。这种新颖的高精度方法可能是检测肌肉突变体中小的被动刚度变化的有效工具。