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Related Concept Videos

Lagging Strand Synthesis01:59

Lagging Strand Synthesis

During replication, the complementary strands in double-stranded DNA are synthesized at different rates. Replication first begins on the leading strand. Replication starts later, occurs more slowly, and proceeds discontinuously on the lagging strand.
There are several major differences between synthesis of the leading strand and synthesis of the lagging strand. 1) Leading strand synthesis happens in the direction of replication fork opening, whereas lagging strand synthesis happens in the...
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...
Homologous Recombination02:31

Homologous Recombination

The basic reaction of homologous recombination (HR) involves two chromatids that contain DNA sequences sharing a significant stretch of identity. One of these sequences uses a strand from another as a template to synthesize DNA in an enzyme-catalyzed reaction. The final product is a novel amalgamation of the two substrates. To ensure an accurate recombination of sequences, HR is restricted to the S and G2 phases of the cell cycle. At these stages, the DNA has been replicated already and the...
The DNA Replication Fork01:02

The DNA Replication Fork

An organism’s genome needs to be duplicated in an efficient and error-free manner for its growth and survival. The replication fork is a Y-shaped active region where two strands of DNA are separated and replicated continuously. The coupling of DNA unzipping and complementary strand synthesis is a characteristic feature of a replication fork.   Organisms with small circular DNA, such as E. coli, often have a single origin of replication; therefore, they have only two replication forks, one in...
Restarting Stalled Replication Forks02:37

Restarting Stalled Replication Forks

DNA replication is initiated at sites containing predefined DNA sequences known as origins of replication. DNA is unwound at these sites by the minichromosome maintenance (MCM) helicase and other factors such as Cdc45 and the associated GINS complex.The unwound single strands are protected by replication protein A (RPA) until DNA polymerase starts synthesizing DNA at the 5’ end of the strand in the same direction as the replication fork. To prevent the replication fork from falling apart, a...
Protein Complex Assembly02:41

Protein Complex Assembly

Proteins can form homomeric complexes with another unit of the same protein or heteromeric complexes with different types.  Most protein complexes self-assemble spontaneously via ordered pathways, while some proteins need assembly factors that guide their proper assembly. Despite the crowded intracellular environment, proteins usually interact with their correct partners and form functional complexes.
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Related Experiment Video

Updated: Jun 2, 2026

Self-assembly of Complex Two-dimensional Shapes from Single-stranded DNA Tiles
10:23

Self-assembly of Complex Two-dimensional Shapes from Single-stranded DNA Tiles

Published on: May 8, 2015

Competing interactions in DNA assembly on graphene.

Saliha Akca1, Ashkan Foroughi, Daniel Frochtzwajg

  • 1Department of Physics and Astronomy, California State University Northridge, Northridge, California, United States of America.

Plos One
|May 3, 2011
PubMed
Summary

Short DNA strands form distinct patterns on graphene. A new model explains this assembly by the competition between base-base and base-graphene interactions, revealing DNA interaction strength.

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Area of Science:

  • Materials Science
  • Biophysics
  • Nanotechnology

Background:

  • Single-stranded DNA (ssDNA) interactions with graphene surfaces are crucial for nanotechnology applications.
  • Existing models fail to explain the observed assembly patterns of ssDNA on graphite.

Purpose of the Study:

  • To investigate the self-assembly patterns of short ssDNA strands on graphene.
  • To develop a new model explaining the observed DNA assembly behavior.

Main Methods:

  • Experimental observation of ssDNA patterns on graphene surfaces.
  • Analysis of existing interaction models (DNA-graphene binding, hydrophobic, base-specific).

Main Results:

  • ssDNA forms two distinct patterns: small spherical particles and elongated networks.
  • A crossover in assembly patterns was observed.
  • A novel model based on competing pi stacking interactions (base-base vs. base-graphene) was proposed.
  • A critical crossover energy of 0.3-0.5 eV was inferred.

Conclusions:

  • The observed ssDNA assembly on graphene is driven by a competition between base-base and base-graphene pi stacking.
  • This study provides a projective measurement of base-base interaction strength.
  • The findings offer insights into DNA-surface interactions for nanoscale design.