Shirakawa I, Chaen S, Bagshaw C R, Sugi H
Department of Physiology, School of Medicine, Teikyo University, Tokyo 173, Japan.
Biophys J. 2000 Feb;78(2):918-26. doi: 10.1016/S0006-3495(00)76649-5.
The kinetics of displacement of a fluorescent nucleotide, 2'(3')-O-[N[2-[[Cy3]amido]ethyl]carbamoyl]-adenosine 5'-triphosphate (Cy3-EDA-ATP), bound to rabbit soleus muscle myofibrils were studied using flash photolysis of caged ATP. Use of myofibrils from this slow twitch muscle allowed better resolution of the kinetics of nucleotide exchange than previous studies with psoas muscle myofibrils (, Biophys. J. 73:2033-2042). Soleus myofibrils in the presence of Cy3-EDA-nucleotides (Cy3-EDA-ATP or Cy3-EDA-ADP) showed selective fluorescence staining of the A-band. The K(m) for Cy3-EDA-ATP and the K(d) for Cy3-EDA-ADP binding to the myofibril A-band were 1.9 microM and 3.8 microM, respectively, indicating stronger binding of nucleotide to soleus cross-bridges compared to psoas cross-bridges (2.6 microM and 50 microM, respectively). After flash photolysis of caged ATP, the A-band fluorescence of the myofibril in the Cy3-EDA-ATP solution under isometric conditions decayed exponentially with a rate constant of 0.045 +/- 0.007 s(-1) (n = 32) at 10 degrees C, which was about seven times slower than that for psoas myofibrils. When a myofibril was allowed to shorten with a constant velocity, the nucleotide displacement rate constant increased from 0.066 s(-1) (isometric) to 0.14 s(-1) at 20 degrees C with increasing shortening velocity up to 0.1 myofibril length/s (V(max), the shortening velocity under no load was approximately 0. 2 myofibril lengths/s). The rate constant was not significantly affected by an isovelocity stretch of up to 0.1 myofibril lengths/s. These results suggest that the cross-bridge kinetics are not significantly affected at higher strain during lengthening but depend on the lower strain during shortening. These data also indicate that the interaction distance between a cross-bridge and the actin filament is at least 16 nm for a single cycle of the ATPase.
利用笼锁ATP的闪光光解技术,研究了与兔比目鱼肌肌原纤维结合的荧光核苷酸2′(3′)-O-[N-[2-[[Cy3]氨基]乙基]氨基甲酰基]-腺苷5′-三磷酸(Cy3-EDA-ATP)的置换动力学。与之前对腰大肌肌原纤维的研究相比,使用这种慢肌纤维的肌原纤维能更好地解析核苷酸交换动力学(《生物物理学杂志》73:2033 - 2042)。在存在Cy3-EDA-核苷酸(Cy3-EDA-ATP或Cy3-EDA-ADP)的情况下,比目鱼肌肌原纤维显示出A带的选择性荧光染色。Cy3-EDA-ATP的K(m)值和Cy3-EDA-ADP与肌原纤维A带结合的K(d)值分别为1.9 microM和3.8 microM,这表明与腰大肌横桥相比(分别为2.6 microM和50 microM),核苷酸与比目鱼肌横桥的结合更强。在笼锁ATP的闪光光解后,在等长条件下,Cy3-EDA-ATP溶液中肌原纤维的A带荧光在10℃下以0.045±0.007 s(-1)(n = 32)的速率常数呈指数衰减,这比腰大肌肌原纤维慢约7倍。当肌原纤维以恒定速度缩短时,在20℃下,随着缩短速度增加至0.1肌原纤维长度/秒(V(max),无负载时的缩短速度约为0.2肌原纤维长度/秒),核苷酸置换速率常数从0.066 s(-1)(等长)增加到0.14 s(-1)。速率常数不受高达0.1肌原纤维长度/秒的等速拉伸的显著影响。这些结果表明,在拉长过程中较高应变下横桥动力学没有显著受到影响,但取决于缩短过程中的较低应变。这些数据还表明,对于ATP酶的单个循环,横桥与肌动蛋白丝之间的相互作用距离至少为16 nm。