Karagiannis Peter, Babu Gopal J, Periasamy Muthu, Brozovich Frank V
Department of Physiology and Biophysics, Case Western Reserve University, Cleveland, OH 44106-4970, USA.
J Physiol. 2003 Mar 1;547(Pt 2):463-73. doi: 10.1113/jphysiol.2002.035717. Epub 2003 Jan 17.
The seven amino acid insert in the smooth muscle myosin heavy chain is thought to regulate the kinetics of contraction, contributing to the differences between fast and slow smooth muscle. The effects of this insert on force and stiffness were determined in bladder tissue of a transgenic mouse line expressing the insert SMB at one of three levels: an SMB wild type (+/+), an SMA homozygous type (-/-) and a heterozygous type (+/-). For skinned muscle, an increase in MgADP or inorganic phosphate (Pi) should shift the distribution of crossbridges in the actomyosin ATPase (AMATPase) to increase the relative population of the crossbridge state prior to ADP release and Pi release, respectively. Exogenous ADP increased force and stiffness in a manner consistent with increasing the Ca2+ concentration in both the +/+ and +/- mouse types. However, the -/- type showed a significantly greater increase in force than in stiffness suggesting that immediately prior to ADP release, the AMATPase either has an additional force producing isomerization state or a slower ADP dissociation rate for the -/- type compared to the +/+ or +/- types. Exogenous Pi led to a significantly greater decrease in stiffness than in force for all three mouse types suggesting that there is a force producing state prior to Pi release. In addition, the increase in Pi showed similar changes in the +/+ and -/- types whereas in the +/- type the decreases in both force and stiffness were greater than the other two mouse types indicating that the insert can affect the cooperativity between myosin heads. In conclusion, the seven amino acid insert modulates the kinetics and/or states of the AMATPase, which could lead to differences in the kinetics of contraction between fast and slow smooth muscle.
平滑肌肌球蛋白重链中的七个氨基酸插入序列被认为可调节收缩动力学,这导致了快、慢平滑肌之间的差异。在一个转基因小鼠品系的膀胱组织中,测定了该插入序列在三种表达水平下对力和硬度的影响:SMB野生型(+/+)、SMA纯合型(-/-)和杂合型(+/-)。对于脱皮肌肉,MgADP或无机磷酸盐(Pi)的增加应会改变肌动球蛋白ATP酶(AMATPase)中横桥的分布,分别增加ADP释放和Pi释放之前横桥状态的相对比例。外源性ADP以与增加Ca2+浓度一致的方式增加了+/+和+/-小鼠类型的力和硬度。然而,-/-类型的力增加幅度明显大于硬度增加幅度,这表明在ADP释放之前,与+/+或+/-类型相比,-/-类型的AMATPase要么具有额外的产生力的异构化状态,要么具有较慢的ADP解离速率。外源性Pi导致所有三种小鼠类型的硬度下降幅度明显大于力的下降幅度,这表明在Pi释放之前存在一种产生力的状态。此外,Pi的增加在+/+和-/-类型中显示出类似的变化,而在+/-类型中,力和硬度的下降幅度均大于其他两种小鼠类型,这表明该插入序列可影响肌球蛋白头部之间的协同作用。总之,七个氨基酸插入序列调节了AMATPase的动力学和/或状态,这可能导致快、慢平滑肌收缩动力学的差异。