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Related Concept Videos

Polytene Chromosomes02:04

Polytene Chromosomes

Polytene chromosomes are giant interphase chromosomes with several DNA strands placed side by side. They were discovered in the year 1881 by Balbiani in salivary glands, intestine, muscles, malpighian tubules, and hypoderm of larvae Chironomus plumosus. Hence, these are also called "Salivary gland chromosomes." These are found in insects of the order Diptera and Collembola; in certain organs of mammals; and synergids, antipodes of flowering plants. Polytene chromosomes are also regularly...
Polytene Chromosomes02:04

Polytene Chromosomes

Polytene chromosomes are giant interphase chromosomes with several DNA strands placed side by side. They were discovered in the year 1881 by Balbiani in salivary glands, intestine, muscles, malpighian tubules, and hypoderm of larvae Chironomus plumosus. Hence, these are also called "Salivary gland chromosomes." These are found in insects of the order Diptera and Collembola; in certain organs of mammals; and synergids, antipodes of flowering plants. Polytene chromosomes are also regularly...
The Nucleosome Core Particle01:12

The Nucleosome Core Particle

Nucleosomes are the DNA-histone complex, where the DNA strand is wound around the histone core. The histone core is an octamer containing two copies of H2A, H2B, H3, and H4 histone proteins.
Nucleosomes, paradoxically, perform two opposite functions simultaneously. On the one hand, their primary aim is to protect the delicate DNA strands from physical damage and help achieve a higher compaction ratio. On the other hand, they must allow polymerase enzymes to access histone-bound DNA during...
The Nucleosome Core Particle02:10

The Nucleosome Core Particle

Nucleosomes are the DNA-histone complex, where the DNA strand is wound around the histone core. The histone core is an octamer containing two copies of H2A, H2B, H3, and H4 histone proteins.
The paradox
Nucleosomes, paradoxically, perform two opposite functions simultaneously. On the one hand, their main responsibility is to protect the delicate DNA strands from physical damage and help achieve a higher compaction ratio. While on the other hand, they must allow polymerase enzymes to access DNA...
Diversity of Protists IV01:27

Diversity of Protists IV

Amoebozoa represent a diverse group of terrestrial and aquatic protists that utilize lobe-shaped pseudopodia for locomotion and feeding. This characteristic differentiates them from the Rhizaria, which possess threadlike pseudopodia. The primary classifications within Amoebozoa include gymnamoebas, entamoebas, and the plasmodial and cellular slime molds. Phylogenetic evidence indicates that Amoebozoa diverged from a lineage that ultimately gave rise to fungi and animals.Gymnamoebas and...
Lampbrush Chromosomes01:51

Lampbrush Chromosomes

In 1882, Flemming observed lampbrush chromosomes (LBC) in salamander eggs. Later in 1892, Rückert observed LBCs in shark egg cells and coined the term "lampbrush chromosomes" because they looked like brushes used to clean kerosene lamps.
LBCs are made up of two pairs of conjugating homologous chromatids. Each chromatid consists of alternatively positioned regions of condensed-inactive chromatin and loosely placed-active side loops, which can be contracted and extended. The loops resemble the...

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Patterning of Microorganisms and Microparticles through Sequential Capillarity-assisted Assembly
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Patterning of Microorganisms and Microparticles through Sequential Capillarity-assisted Assembly

Published on: November 4, 2021

Polygamous particles.

Kun-Ta Wu1, Lang Feng, Ruojie Sha

  • 1Center for Soft Matter Research, Department of Physics, New York University, New York, NY 10003, USA. ktw224@nyu.edu

Proceedings of the National Academy of Sciences of the United States of America
|October 27, 2012
PubMed
Summary
This summary is machine-generated.

Researchers developed "multiflavored" DNA-functionalized particles for programming complex self-assembly. A single particle can bind to dozens of different particle types, enabling novel material structures and properties.

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Area of Science:

  • Materials Science
  • Nanotechnology
  • Biotechnology

Background:

  • DNA's specific binding properties are utilized for programming the self-assembly of micro- and nanoscale particles.
  • Current DNA-functionalized particles primarily bind specific pairs, limiting complex assembly designs.

Purpose of the Study:

  • To design and demonstrate "multiflavored" DNA-functionalized particles capable of binding to multiple distinct particle types.
  • To explore the design rules and limitations for creating particles with numerous binding specificities.

Main Methods:

  • Development of design rules for multiflavored particles using DNA sticky ends.
  • Investigation of the energetic and entropic costs associated with increasing the number of binding flavors.
  • Experimental demonstration using 2-μm colloidal particles functionalized with 11-base sticky ends.

Main Results:

  • A single particle can bind to 40 different particle types within accessible temperature and time regimes.
  • The practical limit for distinct binding sequences is approximately 73, constrained by sequence overlaps and entropic costs.
  • Demonstrated a three-particle system forming either a fluid of clusters or an elastic gel based on cooling rate.

Conclusions:

  • Multiflavored particles significantly expand the possibilities for DNA-programmable self-assembly.
  • This approach enables the creation of complex structures and dynamic materials with tunable properties.
  • The findings pave the way for advanced particle assembly systems with unprecedented control.