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Deciphering nature's remarkable way of encoding functions in its biominerals holds the potential to enable the rational development of nature‐inspired materials with tailored properties. However, the complex processes that convert solution‐state precursors into solid biomaterials remain largely unknown. In this study, an unconventional approach is presented to characterize these precursors for the diatom‐derived peptides R5 and synthetic Silaffin‐1A1(synSil‐1A1). These molecules can form defined supramolecular assemblies in solution, which act as templates for solid silica structures. Using a tailored structural biology toolbox, the structure‐function relationships of these self‐assemblies are unveiled. NMR‐derived constraints are employed to enable a recently developed fractal‐cluster formalism and then reveal the architecture of the peptide assemblies in atomistic detail. Finally, by monitoring the self‐assembly activities during silica formation at simultaneous high temporal and residue resolution using real‐time spectroscopy, the mechanism is elucidated underlying template‐driven silica formation. Thus, it is demonstrated how to exercise morphology control over bioinorganic solids by manipulating the template architectures. It is found that the morphology of the templates is translated into the shape of bioinorganic particles via a mechanism that includes silica nucleation on the solution‐state complexes' surfaces followed by complete surface coating and particle precipitation. [ABSTRACT FROM AUTHOR]

Bioprosthetic heart valves create turbulent flow during early systole which might be detrimental to their durability and performance. Complex mechanisms in the unsteady and heterogeneous flow field complicate the isolation of specific instability mechanisms. We use linear stability analysis and numerical simulations of the flow in a simplified model to study mechanisms initiating the laminar–turbulent transition. The analysis of a modified Orr–Sommerfeld equation, which includes a model for fluid–structure interaction (FSI), indicates Kelvin–Helmholtz and FSI instabilities for a physiological Reynolds number regime. Two-dimensional parametrized FSI simulations confirm the growth rates and phase speeds of these instabilities. The eigenmodes associated with the observed leaflet kinematics allow for decoupled leaflet oscillations. A detailed analysis of the temporal evolution of the flow field shows that the starting vortex interacts with the aortic wall leading to a secondary vortex which moves towards the shear layer in the wake of the leaflets. This appears to be connected to the onset of the shear layer instabilities that are followed by the onset of leaflet motion leading to large-scale vortex shedding and eventually to a nonlinear breakdown of the flow. Numerical results further indicate that a narrower aorta leads to an earlier onset of the shear layer instabilities. They also suggest that the growing perturbations of the shear layer instability propagate upstream and may initiate the FSI instabilities on the valve leaflets. [ABSTRACT FROM AUTHOR]

Microvascular obstruction (MVO) often occurs in ST-elevation myocardial infarction (STEMI) patients after percutaneous coronary intervention (PCI). Diagnosis and treatment of MVO lack appropriate and established procedures. This study focused on two major points by using an in vitro multiscale flow model, which comprised an aortic root model with physiological blood flow and a microfluidic model of the microcirculation with vessel diameters down to 50 µm. First, the influence of porcine microthrombi (MT), injected into the fluidic microchip, on perfusion was investigated. We found that only 43% of all injected MT were fully occlusive. Second, it could also be shown that the maximal concentration of a dye (representing therapeutic agent) during intracoronary infusion could be increased on average by 58%, when proximally occluding the coronary artery by a balloon during drug infusion. The obtained results and insights enhance the understanding of perfusion in MVO-affected microcirculation and could lead to improved treatment methods for MVO patients. [ABSTRACT FROM AUTHOR]