Department of Molecular and Structural Biochemistry, North Carolina State University, Raleigh, North Carolina 27695, USA.
Protein Sci. 2009 Dec;18(12):2500-17. doi: 10.1002/pro.259.
Caspases are vital to apoptosis and exist in the cell as inactive zymogens. Dimerization is central to procaspase activation because the active sites are comprised of loops from both monomers. Although initiator procaspases are stable monomers until activated on cell death scaffolds, the effector caspases, such as procaspase-3, are stable dimers. The activation mechanisms are reasonably well understood in terms of polypeptide chain cleavage and subsequent active site rearrangements in the dimer, but the mechanisms that govern dimer assembly are not known. To further understand procaspase dimerization, we examined the folding and assembly of procaspase-3 by fluorescence emission, circular dichroism, differential quenching by acrylamide, anisotropy, and enzyme activity assays. Single-mixing stopped-flow refolding studies showed a complex burst phase in which multiple monomeric species form rapidly. At longer times, the monomer folds through several intermediates, some of which appear to be off-pathway or misfolded, before eventually forming a dimerization-competent species. Enzyme activity studies demonstrated a slow rate of dimerization (approximately 70 M(-1) s(-1)). In addition, single-mixing stopped-flow unfolding studies revealed a complex unfolding process with a slow rate of dimer dissociation. Interestingly, multiple dimeric species were observed in the burst phase for unfolding, suggesting that the native ensemble consists of at least two major conformations. Collectively, these results demonstrate complex folding and unfolding behavior for procaspase-3 and suggest that slow dimerization results from the lack of stabilizing native contacts in the initial encounter complex.
半胱天冬酶对于细胞凋亡至关重要,以无活性酶原的形式存在于细胞中。二聚化是前半胱天冬酶激活的核心,因为活性位点由两个单体的环组成。尽管起始半胱天冬酶在细胞死亡支架上被激活之前是稳定的单体,但效应半胱天冬酶(如前半胱天冬酶-3)是稳定的二聚体。在多肽链切割和随后的二聚体活性位点重排方面,激活机制已经得到了很好的理解,但控制二聚体组装的机制尚不清楚。为了进一步了解前半胱天冬酶的二聚化,我们通过荧光发射、圆二色性、丙烯酰胺的差分猝灭、各向异性和酶活性测定研究了前半胱天冬酶-3 的折叠和组装。单混合停流重折叠研究显示出一个复杂的爆发相,其中多个单体物种迅速形成。在较长的时间内,单体通过几个中间体折叠,其中一些似乎是偏离途径或错误折叠的,然后最终形成具有二聚化能力的物种。酶活性研究表明二聚化的速率较慢(约 70 M(-1) s(-1))。此外,单混合停流展开研究揭示了一个复杂的展开过程,其解聚速率较慢。有趣的是,在展开的爆发相中观察到了多种二聚体物种,这表明天然聚集体至少由两种主要构象组成。总的来说,这些结果表明前半胱天冬酶-3 的折叠和展开行为复杂,并表明缓慢的二聚化是由于初始接触复合物中缺乏稳定的天然接触所致。