Modeling DNA Resonance
Max Myakishev-Rempel, DNA Resonance Research Foundation, San Diego, CA, USA
Abstract
We propose that DNA serves as the main resonator in biological tissues for ultraweak bioluminescence emission and reception. DNA possesses three key properties that make it an ideal candidate for this role: its highly structured double helix, its dynamic nature through breathing modes and chromatin remodeling, and its genomic code that defines both cellular function and tissue morphogenesis.
Our model suggests that DNA sequences imprint information onto surrounding water molecules through their three-dimensional structure. To test whether chromatin threads couple through sequence-specific homological interactions, we analyzed chromatin conformation capture experiments. The analysis confirmed that homologous DNA sequences preferentially couple during chromatin folding, revealing significant enrichment at ligation points.
This sequence-specific homological coupling provides the key to understanding how functional structures form and evolve in biological systems. These structures dynamically evolve as chromatin threads rearrange through homology-driven interactions, creating ever-changing resonant architectures. The chromatin architecture created through these interactions forms liquid crystalline structures that can vibrate at specific frequencies. These vibrating liquid crystal domains represent the physical basis for biological resonance phenomena. The specific folding patterns determined by sequence homology generate characteristic vibrational signatures that produce ultraweak photon emission from tissues. Since weak electromagnetic fields play regulatory roles in physiological processes, our findings provide a mechanism connecting DNA sequence to dynamic chromatin structures to endogenous biophotonic emission.
Speaker
Max Myakishev-Rempel
DNA Resonance Research Foundation
United States
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