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Hybridization of Atomic Orbitals I03:24

Hybridization of Atomic Orbitals I

The mathematical expression known as the wave function, ψ, contains information about each orbital and the wavelike properties of electrons in an isolated atom. When atoms are bound together in a molecule, the wave functions combine to produce new mathematical descriptions that have different shapes. This process of combining the wave functions for atomic orbitals is called hybridization and is mathematically accomplished by the linear combination of atomic orbitals. The new orbitals that...
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sp3d and sp3d 2 Hybridization
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According to valence bond theory, a covalent bond results when: (1) an orbital on one atom overlaps an orbital on a second atom, and (2) the single electrons in each orbital combine to form an electron pair. The strength of a covalent bond depends on the extent of overlap of the orbitals involved. Maximum overlap is possible when the orbitals overlap on a direct line between the two nuclei.
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Updated: Jun 5, 2026

Split Hybridization Probe Utilizing a DNA Fluorescent Light-up Aptamer as a Signal Reporter for Sequence-Specific Nucleic Acid Analysis
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Competitive hybridization models.

Vera Cherepinsky1, Ghazala Hashmi, Bud Mishra

  • 1Department of Mathematics and Computer Science, Fairfield University, Fairfield, Connecticut 06824, USA. vcherepinsky@fairfield.edu

Physical Review. E, Statistical, Nonlinear, and Soft Matter Physics
|January 15, 2011
PubMed
Summary
This summary is machine-generated.

Multiplexed microarray experiments can yield variable results due to probe competition for targets. A new physical model predicts these effects, improving experimental design for DNA analysis and genotyping.

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Published on: May 27, 2020

Area of Science:

  • Molecular Biology
  • Bioinformatics
  • Genomics

Background:

  • Microarray technology enables DNA abundance measurement via hybridization of targets to probes on a surface.
  • A key assumption in multiplexed microarray analysis is that probe performance is independent of other probes present.
  • This assumption is often violated due to complex probe interactions, leading to signal variability.

Purpose of the Study:

  • To develop a detailed physical model of DNA hybridization in multiplexed microarray reactions.
  • To understand and predict probe competition for target molecules, especially under limited target conditions.
  • To enhance the design and efficiency of microarray-based experiments.

Main Methods:

  • A physical model based on ordinary differential equations (ODEs) describing kinetic mass action was developed.
  • The model incorporates conservation-of-mass equations to simulate pairwise probe interactions and competition.
  • Affinity constants were calculated from thermodynamic parameters using the nearest-neighbor (NN) model to predict hybridization free energy.

Main Results:

  • Simulations revealed predictable 'competition' effects between probes for limited targets.
  • These competitive effects are dependent on the affinity constants of match and mismatch sequences.
  • The model successfully explains observed signal variability when probes are analyzed individually versus in parallel.

Conclusions:

  • The competitive hybridization model provides insights into probe interactions in multiplexed arrays.
  • Simulation results aid in optimizing experiment design and probe pooling strategies.
  • This approach can improve accuracy in genotyping (e.g., HLA, SNP, CNV) and mutation detection (e.g., cystic fibrosis, cancer).