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Related Concept Videos

Assembly of Complex Microtubule Structures01:32

Assembly of Complex Microtubule Structures

Complex microtubule structures are present in resting cells and in dividing cells. In resting cells, they are responsible for maintaining the cellular architecture, tracks for intracellular transport, positioning of organelles, assembly of cilia and flagella. They mediate the bipolar spindle assembly for chromosomal segregation and positioning of the cell division plate in dividing cells. The formation of microtubule complex structures depends on the cell type, cell stage, and cell function.
Assembly of Cytoskeletal Filaments01:18

Assembly of Cytoskeletal Filaments

Cytoskeletal filaments are polymeric forms of smaller protein subunits. However, individual cytoskeletal filaments may easily disassemble or associate with other similar filaments to form rigid structures. Microfilaments, made of actin monomers, rely on actin-binding proteins to form bundles and create networks of individual actin filaments. Microtubules rely on microtubule-associated proteins (MAPs) to form sturdy cylindrical structures. However, the proteins involved in forming complex...
Spindle Assembly02:50

Spindle Assembly

Spindle assembly occurs through three, often coexisting, pathways – the centrosome-mediated pathway, the chromatin-mediated pathway, and the microtubule-mediated pathway – collectively contributing to form a robust spindle apparatus.
In most cells, centrosomes are the primary microtubule nucleation centers. In the centrosome-mediated pathway, the G2-prophase transition triggers centrosome maturation and increased microtubule nucleation. Progressive nucleation results in a microtubule array...
Mechanism of Lamellipodia Formation01:31

Mechanism of Lamellipodia Formation

Cells migrating in response to external stimuli form lamellipodia, which are thin membrane protrusions supported by a mesh of linked, branched, or unbranched actin filaments. These actin filaments interact with myosin motor proteins, creating the dynamic actomyosin complex within the cytoskeleton. Contractility, or the ability to generate contractile stress, is inherent to the actomyosin complex. It helps cells detect the stiffness of the surrounding ECM and exert contractile force for...
Formation of Higher-order Actin Filaments01:11

Formation of Higher-order Actin Filaments

The polymerization of G-actin monomers into filamentous F-actin is a multi-step process. Once the F-actins are formed, they can bundle together in different arrangements to form higher-order networks and regulate cellular functions. Common examples include the formation of lamellipodia and filopodia at the cell's leading edge by actin reorganization in a migrating cell. The microvilli on the brush border epithelial cells are also formed through the F-actin network.
The high-order actin networks...
Generation of Straight or Branched Actin Filaments01:14

Generation of Straight or Branched Actin Filaments

The straight or branched structure formation of actin filaments is controlled by nucleating proteins such as the formins and Arp2/3 complex. Formin-mediated assembly results in straight filaments, whereas Arp2/3 protein complex-mediated assembly results in branched actin filaments.
Arp2/3 Complex
Arp2/3 complex is a seven-subunit complex consisting of two proteins similar to actin- Arp2 and Arp3, and five other subunits that help keep Arp2 and Arp3 inactive. When required, the complex is...

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Patterning of Microorganisms and Microparticles through Sequential Capillarity-assisted Assembly
10:17

Patterning of Microorganisms and Microparticles through Sequential Capillarity-assisted Assembly

Published on: November 4, 2021

Nonclassical assembly pathways of anisotropic particles.

Stephen Whitelam1

  • 1Molecular Foundry, Lawrence Berkeley National Laboratory, 1 Cyclotron Road, Berkeley, California 94720, USA. swhitelam@lbl.gov

The Journal of Chemical Physics
|May 27, 2010
PubMed
Summary

Anisotropic particles can self-assemble into complex structures through nonclassical pathways, driven by thermodynamics or dynamics. This research provides a framework for predicting these intricate self-assembly behaviors.

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Area of Science:

  • Materials Science
  • Chemical Physics
  • Nanotechnology

Background:

  • Recent advances in synthetic methods yield diverse nanoparticles and bio-inspired molecules with anisotropic shapes.
  • Experimental studies reveal nonclassical self-assembly pathways in these particles, forming ordered structures via intermediates distinct from the bulk material.

Purpose of the Study:

  • To investigate the thermodynamic and dynamic driving forces behind nonclassical self-assembly of anisotropic particles.
  • To develop a predictive framework for understanding complex self-assembly behaviors.

Main Methods:

  • Application of mean field theory to a model of interacting anisotropic particles.
  • Analysis of parameter space to identify regimes governed by thermodynamics versus dynamics.

Main Results:

  • A clear thermodynamic impetus for nonclassical ordering was identified in specific parameter regimes.
  • In other regimes, assembly pathways were found to be predominantly selected by dynamics.

Conclusions:

  • The study demonstrates that both thermodynamics and dynamics play crucial roles in directing the self-assembly of anisotropic particles.
  • This theoretical approach offers a method to predict when complex, nonclassical self-assembly pathways will be favored over classical nucleation theory.