Sowa Glenna Z, Cannell David S, Liu Andrea J, Reisler Emil
Department of Chemistry and Biochemistry, University of California Los Angeles, Los Angeles, California 90095, USA.
J Phys Chem B. 2006 Nov 9;110(44):22279-84. doi: 10.1021/jp063371w.
To better understand the mechanism of actin filament (F-actin) bundling by polyamines, we have measured the onset of bundling as a function of polyamine concentration. Samples were centrifuged at low speeds to separate bundles from unbundled actin, and the relative amounts of actin in the pellet and supernatant were determined via gel electrophoresis, yielding a description of the bundling transition as a function of actin and polyamine concentrations. These experiments were carried out for two different polyamines, spermine (tetravalent) and spermidine (trivalent). We found that the threshold concentration of polyamine needed to bundle actin is independent of both actin concentration and Mg2+ concentration over a wide range in Mg2+ concentration. We also find that spermine in F-actin bundles is essentially invisible in solution-phase proton NMR, suggesting that it is bound so tightly to F-actin that it is immobilized.
为了更好地理解多胺对肌动蛋白丝(F-肌动蛋白)的成束机制,我们测量了成束起始情况与多胺浓度的函数关系。样品以低速离心,将成束的肌动蛋白与未成束的肌动蛋白分离,通过凝胶电泳测定沉淀和上清液中肌动蛋白的相对含量,从而得到成束转变与肌动蛋白和多胺浓度的函数关系描述。对两种不同的多胺,即精胺(四价)和亚精胺(三价)进行了这些实验。我们发现,在较宽的Mg2+浓度范围内,使肌动蛋白成束所需的多胺阈值浓度与肌动蛋白浓度和Mg2+浓度均无关。我们还发现,F-肌动蛋白束中的精胺在溶液相质子核磁共振中基本不可见,这表明它与F-肌动蛋白结合得非常紧密以至于被固定住了。