Anson M, Drummond D R, Geeves M A, Hennessey E S, Ritchie M D, Sparrow J C
National Institute for Medical Research, Mill Hill, London, United Kingdom.
Biophys J. 1995 May;68(5):1991-2003. doi: 10.1016/S0006-3495(95)80376-0.
Two missense mutations of the flight muscle-specific actin gene of Drosophila melanogaster, Act88F, assemble into normally structured myofibrils but affect the flight ability of flies and the mechanical kinetics of isolated muscle fibers. We describe the isolation of actin from different homozygous Act88F strains, including wild-type, an Act88F null mutant (KM88), and two Act88F single point mutations (E316K and G368E), their biochemical interactions with rabbit myosin subfragment 1 (S1), and behavior with rabbit myosin and heavy meromyosin in in vitro motility assays. The rabbit and wild-type Drosophila actins have different association rate constants with S1 (2.64 and 1.77 microM-1 s-1, respectively) and in vitro motilities (2.51, 1.60 microns s-1) clearly demonstrating an isoform-specific difference. The G368E mutation shows a reduced affinity for rabbit S1 compared with the wild type (increasing from 0.11 to 0.17 microM) and a reduced velocity in vitro (reduced by 19%). The E316K mutant actin has no change in affinity for myosin S1 or in vitro motility with heavy meromyosin but does have a reduced in vitro motility (15%) with myosin. These results are discussed with respect to the recently published atomic models for the actomyosin structure and our findings that G368E fibers show a reduced rate constant for delayed tension development and increased fiber stiffness. We interpret these results as possibly caused either by effects on A1 myosin light chain binding or conformational changes within the subdomain 1 of actin, which contains the myosin binding site. E316K is discussed with respect to its likely position within the tropomyosin binding site of actin.
黑腹果蝇飞行肌特异性肌动蛋白基因Act88F的两个错义突变,能组装成结构正常的肌原纤维,但会影响果蝇的飞行能力以及分离出的肌纤维的机械动力学。我们描述了从不同纯合Act88F菌株中分离肌动蛋白的过程,这些菌株包括野生型、Act88F无效突变体(KM88)以及两个Act88F单点突变体(E316K和G368E),还描述了它们与兔肌球蛋白亚片段1(S1)的生化相互作用,以及在体外运动分析中与兔肌球蛋白和重酶解肌球蛋白的行为。兔肌动蛋白和野生型果蝇肌动蛋白与S1的缔合速率常数不同(分别为2.64和1.77微摩尔⁻¹秒⁻¹),体外运动速度也不同(分别为2.51、1.60微米秒⁻¹),这清楚地表明了同工型特异性差异。与野生型相比,G368E突变体对兔S1的亲和力降低(从0.11增加到0.17微摩尔),体外速度降低(降低了19%)。E316K突变体肌动蛋白对肌球蛋白S1的亲和力或与重酶解肌球蛋白的体外运动能力没有变化,但与肌球蛋白的体外运动能力降低了(15%)。结合最近发表的肌动球蛋白结构原子模型以及我们的发现(G368E纤维显示延迟张力发展的速率常数降低且纤维硬度增加)对这些结果进行了讨论。我们将这些结果解释为可能是由于对A1肌球蛋白轻链结合的影响或肌动蛋白亚结构域1内的构象变化所致,该亚结构域1包含肌球蛋白结合位点。还讨论了E316K在肌动蛋白原肌球蛋白结合位点内可能的位置。