Nyland L R, Maughan D W
Department of Molecular Physiology and Biophysics, University of Vermont, Burlington, Vermont 05405, USA.
Biophys J. 2000 Mar;78(3):1490-7. doi: 10.1016/S0006-3495(00)76702-6.
Atomic force microscopy was used to investigate the surface morphology and transverse stiffness of myofibrils from Drosophila indirect flight muscle exposed to different physiologic solutions. I- and A-bands were clearly observed, and thick filaments were resolved along the periphery of the myofibril. Interfilament spacings correlated well with estimates from previous x-ray diffraction studies. Transverse stiffness was measured by using a blunt tip to indent a small section of the myofibrillar surface in the region of myofilament overlap. At 10 nm indention, the effective transverse stiffness (K( perpendicular)) of myofibrils in rigor solution (ATP-free, pCa 4.5) was 10.3 +/- 5.0 pN nm(-1) (mean +/- SEM, n = 8); in activating solution (pCa 4.5), 5.9 +/- 3.1 pN nm(-1); and in relaxing solution (pCa 8), 4.4 +/- 2.0 pN nm(-1). The apparent transverse Young's modulus (E( perpendicular)) was 94 +/- 41 kPa in the rigor state and 40 +/- 17 kPa in the relaxed state. The value of E( perpendicular) for calcium-activated myofibrils (55 +/- 29 kPa) was approximately a tenth that of Young's modulus in the longitudinal direction, a difference that at least partly reflects the transverse flexibility of the myosin molecule.
原子力显微镜被用于研究暴露于不同生理溶液中的果蝇间接飞行肌肌原纤维的表面形态和横向刚度。清晰观察到了明带和暗带,并且沿着肌原纤维的周边分辨出了粗肌丝。丝间间距与先前X射线衍射研究的估计值高度相关。通过使用钝头在肌丝重叠区域压痕一小段肌原纤维表面来测量横向刚度。在10纳米压痕时,处于僵直溶液(无ATP,pCa 4.5)中的肌原纤维的有效横向刚度(K(垂直))为10.3±5.0皮牛·纳米⁻¹(平均值±标准误,n = 8);在激活溶液(pCa 4.5)中为5.9±3.1皮牛·纳米⁻¹;在松弛溶液(pCa 8)中为4.4±2.0皮牛·纳米⁻¹。在僵直状态下,表观横向杨氏模量(E(垂直))为94±41千帕,在松弛状态下为40±17千帕。钙激活肌原纤维的E(垂直)值(55±29千帕)约为纵向杨氏模量的十分之一,这种差异至少部分反映了肌球蛋白分子的横向柔韧性。