Bio Focus: Complex microstructures emerge from chirality and competitive restrictions
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C
rystals are generally perceived as objects exhibiting long-range atomic symmetry with overall simple morphologies. As an example, rock salt has a cubic crystallographic structure. Grains of salt encountered in daily life have visibly smooth surfaces. With this perception, morphological complexity in crystals is difficult to imagine and explain. However, sea urchins and marine organisms called coccolithophores display morphological complexity while containing single-crystal components with intricate geometrical shapes. The emergence and existence of such complex geometry in these biological crystals has remained a biomineralization mystery. The surprise stems from the fact that these organisms do not grow from highly defined and size-disperse nanoscale components and, therefore, the wide size distribution is expected to result in disorganized structures. Entropic and enthalpic considerations would further favor random and compact aggregates lacking any morphological distinction.
A team of researchers led by Nicholas A. Kotov at the University of Michigan has now taken a major step toward addressing this question. Kotov says that the study was prompted by the need to better understand the origin of the complexity of inorganic and composite structures in living organisms. “They have to deal with quite ‘messy’ building blocks with wide size distributions, yet demonstrate amazing sophistication in shapes and functions while having very limited means and resources.” In the study reported in Science (doi:10.1126/science.aaz7949), the researchers looked at “chirality” as the potential key enabler of complexity in microparticles. An object is said to be chiral if it is distinct from its mirror image, such as the clockwise-counterclockwise “flavors” of a molecule. To enable complex structures, nanosheets of gold thiolate were synthesized with their surfaces capped with cysteine as ligand molecules. Cysteine is a chiral amino acid that comes in L- (clockwise) and D- (counterclockwise) flavors. Using either of L- or D-cysteine, chiral nanosheets were realized that aggregated to give surprisingly complex spiky spheres. On the other hand, using L- and D-cysteine ligands simultaneously resulted in flat nanosheets
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Scanning electron micrographs (SEMs) of microparticles formed by aggregation of (a) L-cysteine capped (Au-L-Cys), (b) D-cysteine capped (Au-D-Cys), and (c) L,D-cysteine capped (Au-DL-Cys) gold thiolate nanosheets. (d–f) Enlarged SEMs of (a–c), respectively. (g–i) SEMs of segments of these microparticles with corresponding schematics illustrating their chirality. Credit: Science, AAAS, Wenfeng Jiang, The Kotov Lab, University of Michigan.
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that lacked chirality and led to relatively less complex and flatter morphologies. “The communities of nanoparticles have to develop complex structures in order to satisfy multiple competitive interactions and restrictions that are imposed on the assembly process. It turns out that in this process, the polydispersity matters less than the symmetry of
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