Aizenberg J, Ilan M, Weiner S, Addadi L
Dept. of Structural Biology, Weizmann Institute of Science, Rehovot, Israel.
Connect Tissue Res. 1996;34(4):255-61. doi: 10.3109/03008209609005269.
Control over the shapes of biologically formed crystals is generally not well understood. We have studied the morphogenesis of the different-shaped calcareous sponge spicules using high-resolution synchrotron X-ray diffraction. We show that a remarkable correlation exists between the distribution of defects within spicule crystals at the nanometer level and their macroscopic morphologies at the millimeter level. These defects are produced by controlled intercalation of specialized macromolecules into the crystals. We also show that such intracrystalline macromolecules are involved in the regulation of the shapes of synthetic crystals grown de novo from solution, and epitaxially overgrown on the spicule surfaces. We conclude that intracrystalline macromolecules play an important role in modulation of the morphologies of the forming biogenic crystals. Possible mechanisms that may account for the observed growth patterns are supported by fluorescence labeling experiments in vivo.
对生物形成晶体形状的控制通常还未得到很好的理解。我们利用高分辨率同步加速器X射线衍射研究了不同形状的钙质海绵骨针的形态发生。我们表明,在纳米级骨针晶体内缺陷的分布与毫米级宏观形态之间存在显著相关性。这些缺陷是由特定大分子可控地插入晶体中产生的。我们还表明,这种晶内大分子参与了从溶液中重新生长以及在骨针表面外延过度生长的合成晶体形状的调节。我们得出结论,晶内大分子在调节正在形成的生物源晶体形态方面发挥着重要作用。体内荧光标记实验支持了可能解释所观察到生长模式的机制。