Collins Agnieszka, Huang Renjian, Jensen Mikkel Herholdt, Moore Jeffrey R, Lehman William, Wang Chih-Lueh Albert
Boston University School of Medicine; Boston; MA USA.
Bioarchitecture. 2011 May;1(3):127-133. doi: 10.4161/bioa.1.3.16714.
We have previously reported that actin undergoes a conformational transition (which we named "maturation") during polymerization, and that the actin-binding protein, caldesmon (CaD), when added at an early phase of polymerization, interferes with this process (Huang et al. J Biol Chem 2010; 285:71). The pre-transition filament is characterized by relatively low pyrene-fluorescence intensity when pyrene-labeled actin is used as a reporter of subunit assembly into filaments, whereas the mature filament emits a characteristic enhanced fluorescence. Previously reported co-sedimentation experiments suggest that filament formation is not inhibited by the presence of CaD, despite blocking the transition associated with filament maturation. In this study we visualized structural effects of CaD on the assembly of actin filaments by TIRF and electron microscopy. CaD-free actin forms "rough" filaments with irregular edges and indistinct subunit organization during the initial phase (∼20 min under our conditions) of polymerization as reported previously by others (Steinmetz et al. J Cell Biol 1997; 138:559; Galinska-Rakoczy et al. J Mol Biol 2009; 387:869), which most likely correspond to the pre-transition state preceding the maturation step. Later during the polymerization process "mature" filaments exhibit a smoother F-actin appearance with easily detectible double helically arranged actin subunits. While the inclusion of the actin-binding domain of CaD during actin polymerization does not affect the elongation rate, it is associated with a prolonged pre-transition phase, characterized by a delayed alteration (rough to smooth) of the appearance of filaments, consistent with a later onset of the maturation process.
我们之前报道过,肌动蛋白在聚合过程中会经历一种构象转变(我们称之为“成熟”),并且肌动蛋白结合蛋白钙调蛋白(CaD)在聚合早期添加时会干扰这一过程(Huang等人,《生物化学杂志》2010年;285:71)。当使用芘标记的肌动蛋白作为亚基组装成丝的报告分子时,转变前的丝以相对较低的芘荧光强度为特征,而成熟的丝则发出特征性的增强荧光。先前报道的共沉降实验表明,尽管CaD会阻断与丝成熟相关的转变,但丝的形成并不受其存在的抑制。在本研究中,我们通过全内反射荧光显微镜(TIRF)和电子显微镜观察了CaD对肌动蛋白丝组装的结构影响。如其他人之前所报道的(Steinmetz等人,《细胞生物学杂志》1997年;138:559;Galinska-Rakoczy等人,《分子生物学杂志》2009年;387:869),在我们的条件下,聚合初始阶段(约20分钟),不含CaD的肌动蛋白形成边缘不规则且亚基组织不清晰的“粗糙”丝,这很可能对应于成熟步骤之前的转变前状态。在聚合过程后期,“成熟”的丝呈现出更光滑的F-肌动蛋白外观,其肌动蛋白亚基呈易于检测的双螺旋排列。虽然在肌动蛋白聚合过程中包含CaD的肌动蛋白结合结构域不会影响伸长率,但它与延长的转变前阶段相关,其特征是丝外观的改变(从粗糙到光滑)延迟,这与成熟过程的延迟开始一致。