Chang Eric P, Roncal-Herrero Teresa, Morgan Tamara, Dunn Katherine E, Rao Ashit, Kunitake Jennie A M R, Lui Susan, Bilton Matthew, Estroff Lara A, Kröger Roland, Johnson Steven, Cölfen Helmut, Evans John Spencer
Center for Skeletal Biology, Laboratory for Chemical Physics, New York University College of Dentistry , New York, New York 10010, United States.
Department of Physics, University of York , Heslington, York, United Kingdom.
Biochemistry. 2016 Apr 26;55(16):2401-10. doi: 10.1021/acs.biochem.6b00163. Epub 2016 Apr 13.
In the nacre or aragonite layer of the mollusk shell, proteomes that regulate both the early stages of nucleation and nano-to-mesoscale assembly of nacre tablets from mineral nanoparticle precursors exist. Several approaches have been developed to understand protein-associated mechanisms of nacre formation, yet we still lack insight into how protein ensembles or proteomes manage nucleation and crystal growth. To provide additional insights, we have created a proportionally defined combinatorial model consisting of two nacre-associated proteins, C-RING AP7 (shell nacre, Haliotis rufescens) and pseudo-EF hand PFMG1 (oyster pearl nacre, Pinctada fucata), whose individual in vitro mineralization functionalities are well-documented and distinct from one another. Using scanning electron microscopy, flow cell scanning transmission electron microscopy, atomic force microscopy, Ca(II) potentiometric titrations, and quartz crystal microbalance with dissipation monitoring quantitative analyses, we find that both nacre proteins are functionally active within the same mineralization environments and, at 1:1 molar ratios, synergistically create calcium carbonate mesoscale structures with ordered intracrystalline nanoporosities, extensively prolong nucleation times, and introduce an additional nucleation event. Further, these two proteins jointly create nanoscale protein aggregates or phases that under mineralization conditions further assemble into protein-mineral polymer-induced liquid precursor-like phases with enhanced ACC stabilization capabilities, and there is evidence of intermolecular interactions between AP7 and PFMG1 under these conditions. Thus, a combinatorial model system consisting of more than one defined biomineralization protein dramatically changes the outcome of the in vitro biomineralization process.
在软体动物贝壳的珍珠层或文石层中,存在着调节成核早期阶段以及由矿物纳米颗粒前体形成珍珠层片的纳米到中尺度组装的蛋白质组。已经开发了几种方法来理解与珍珠层形成相关的蛋白质机制,但我们仍然缺乏对蛋白质集合或蛋白质组如何控制成核和晶体生长的深入了解。为了提供更多见解,我们创建了一个按比例定义的组合模型,该模型由两种与珍珠层相关的蛋白质组成,即C-RING AP7(红鲍贝壳珍珠层)和假EF手型PFMG1(马氏珠母贝珍珠层),它们各自的体外矿化功能已有充分记录且彼此不同。通过扫描电子显微镜、流动池扫描透射电子显微镜、原子力显微镜、Ca(II)电位滴定以及带有耗散监测定量分析的石英晶体微天平,我们发现这两种珍珠层蛋白在相同的矿化环境中都具有功能活性,并且在1:1摩尔比时,协同形成具有有序晶内纳米孔隙率的碳酸钙中尺度结构,显著延长成核时间,并引发额外的成核事件。此外,这两种蛋白质共同形成纳米级蛋白质聚集体或相,在矿化条件下进一步组装成具有增强的无定形碳酸钙(ACC)稳定能力的蛋白质-矿物聚合物诱导的类似液体前体的相,并且有证据表明在这些条件下AP7和PFMG1之间存在分子间相互作用。因此,由不止一种定义的生物矿化蛋白组成的组合模型系统极大地改变了体外生物矿化过程的结果。