MacLean-Fletcher S, Pollard T D
Cell. 1980 Jun;20(2):329-41. doi: 10.1016/0092-8674(80)90619-4.
Substoichiometric cytochalasin B (CB) inhibits both the rate of actin polymerization and the interaction of actin filaments in solution. The polymerization rate is reduced by inhibition of actin monomer addition to the "barbed" end of the filaments where monomers normally add more rapidly. 2 microM CB reduces the polymerization rate by up to 90%, but has little effect on the rate of monomer addition at the slow ("pointed") end of the filaments and no effect on the rate of filament annealing. Under most ionic conditions tested, 2 microM CB reduces the steady state high shear viscosity by 10-20% and increases the steady state monomer concentration by a factor of 2.5 or less. In addition to the effects on the polymerization process, 2 microM CB strongly reduces the low shear viscosity of actin filaments alone and actin filaments cross-linked by a variety of macromolecules. This may be due to inhibition of actin filament-filament interactions which normally contribute to network formation. Since the inhibition of monomer addition and of actin filament network formation have approximately the same CB concentration dependence, a common CB binding site, probably the barbed end of the filament, may be responsible for both effects.
亚化学计量的细胞松弛素B(CB)可抑制肌动蛋白聚合速率以及溶液中肌动蛋白丝之间的相互作用。聚合速率的降低是由于肌动蛋白单体添加到丝的“刺”端受到抑制,而在该末端单体通常添加得更快。2微摩尔的CB可使聚合速率降低多达90%,但对丝的慢(“钝”)端的单体添加速率影响很小,对丝退火速率没有影响。在大多数测试的离子条件下,2微摩尔的CB可使稳态高剪切粘度降低10 - 20%,并使稳态单体浓度增加2.5倍或更低。除了对聚合过程的影响外,2微摩尔的CB还强烈降低单独的肌动蛋白丝以及由多种大分子交联的肌动蛋白丝的低剪切粘度。这可能是由于抑制了通常有助于网络形成的肌动蛋白丝 - 丝之间的相互作用。由于单体添加抑制和肌动蛋白丝网络形成抑制具有大致相同的CB浓度依赖性,一个共同的CB结合位点,可能是丝的刺端,可能对这两种效应都负责。