Publications by authors named "B Tyukodi"

Article Synopsis
  • The study explores how principles from viral capsid assembly can be applied to create programmable, size-controlled polyhedral shapes that resemble certain cubic structures, like Primitive, Diamond, and Gyroid surfaces.
  • By using design methods from DNA origami, the research shows that as the complexity of these polyhedral assemblies increases, the number of distinct building blocks required remains efficient, similar to viral structures.
  • Simulation tests reveal that achieving both efficient assembly and high accuracy requires a moderate flexibility in the angles and lengths of the components, highlighting a tradeoff between design efficiency and assembly precision due to potential defects.
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Hepatitis B virus (HBV) is an endemic, chronic virus that leads to 800000 deaths per year. Central to the HBV lifecycle, the viral core has a protein capsid assembled from many copies of a single protein. The capsid protein adopts different (quasi-equivalent) conformations to form icosahedral capsids containing 180 or 240 proteins: = 3 or = 4, respectively, in Caspar-Klug nomenclature.

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In contrast to most self-assembling synthetic materials, which undergo unbounded growth, many biological self-assembly processes are self-limited. That is, the assembled structures have one or more finite dimensions that are much larger than the size scale of the individual monomers. In many such cases, the finite dimension is selected by a preferred curvature of the monomers, which leads to self-closure of the assembly.

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We use computational modeling to investigate the assembly thermodynamics of a particle-based model for geometrically frustrated assembly, in which the local packing geometry of subunits is incompatible with uniform, strain-free large-scale assembly. The model considers discrete triangular subunits that drive assembly toward a closed, hexagonal-ordered tubule, but have geometries that locally favor negative Gaussian curvature. We use dynamical Monte Carlo simulations and enhanced sampling methods to compute the free energy landscape and corresponding self-assembly behavior as a function of experimentally accessible parameters that control assembly driving forces and the magnitude of frustration.

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The ability to design and synthesize ever more complicated colloidal particles opens the possibility of self-assembling a zoo of complex structures, including those with one or more self-limited length scales. An undesirable feature of systems with self-limited length scales is that thermal fluctuations can lead to the assembly of nearby, off-target states. We investigate strategies for limiting off-target assembly by using multiple types of subunits.

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