A typical human cell consists of 10,000 different proteins where all biological processes within a cell, tissue or organism depend on selective interactions between them and their targets such as other proteins, DNA regulatory segments or small molecules.
Proteins are linear sequences of 20 different amino acids, and their unique three-dimensional structure transcribed and translated from the DNA determines their biological function.
So what is it that enabled the tens of thousands of different kinds of molecules in the organism to recognize their specific targets?
The classical “lock and key” or its modified “induced fit” models assumes that in the extremely crowded environment of the cell (where there are billions of molecules) by random collisions those molecules that have complementary shapes lock onto to each other so the appropriate biochemical reactions can take place.
This random collision approach also supposed to explain how enzymes can recognize their respective substrates, how antibodies in the immune system can grab onto specific foreign invaders and disarm them and how proteins can dock with different partner proteins or latch onto specific nucleic acids to control gene expression etc.
Prof Irena Cosic showed in her extensive research that all protein sequences with the common biological function have common characteristic frequency component in the distribution of free energy of electrons along the protein backbone that is related to the protein’s biological function.
Furthermore, it was shown that the proteins and their targets have the same characteristic frequency in common that can be used for recognition and interaction between the particular protein and its target at the distance.
Thus, protein interactions can be considered as resonant energy transfer between the interacting molecules and by applying an electromagnetic field, it is possible to program, predict, design and modify proteins and their bioactivity.
Considerable experimental evidence today points to the possibility of modulating biological functions and structures in a controlled way by applying electromagnetic fields.
This phenomenon has been observed and used by Dr Gorgun since the 1970s when he made his key discovery of calculating the resonant frequency of any given molecule per the “Method of Gorgun”.
GEMM is based on the principle of applying the precisely determined electromagnetic fields to the target proteins at the selected resonant frequency to regulate the malfunctioning biological process in a controlled fashion.
A comprehensive description of the method and its effects on neoplastic cells is provided in Dr Gorgun's article "Studies on the Interaction Between Electromagnetic Fields and Living Matter Neoplastic Cell Culture" appeared at the Journal of Frontier Perspectives. |
