Medical Radio activated rhodopsin-like protein?

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The discussion centers on the theoretical possibility of using viral transfection to create brain cells that respond to radio frequency signals, akin to how channelrhodopsin proteins react to light. The feasibility of synthesizing such proteins raises concerns about the potential for controlling populations through radio transmitter towers. However, participants highlight significant scientific challenges. The activation energy required for a hypothetical radio-sensitive rhodopsin would be too low, making it susceptible to thermal energy at human body temperature, thus rendering it ineffective for selective activation. The conversation emphasizes that the laws of physics limit the functionality of proteins in response to electromagnetic signals, particularly outside the visible spectrum. Overall, the idea of large-scale control through engineered proteins responding to radio frequencies is deemed highly unlikely and impractical.
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Just a thought. We have the capability to use viral transfection to stimulate brain cells into producing channelrhodopsin proteins which cause the brain cell to fire in response to a light impulse of a specific frequency. If neuroscientists were able to synthesize a protein with similar function, but which responded to radio frequency signals, and also decided to disperse the viral vector globally, would they basically be capable of controlling the entire infected population through radio transmitter towers? What would you estimate is the likelihood of such a thing happening?
 
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sammysoil said:
Just a thought. We have the capability to use viral transfection to stimulate brain cells into producing channelrhodopsin proteins which cause the brain cell to fire in response to a light impulse of a specific frequency. If neuroscientists were able to synthesize a protein with similar function, but which responded to radio frequency signals, and also decided to disperse the viral vector globally, would they basically be capable of controlling the entire infected population through radio transmitter towers? What would you estimate is the likelihood of such a thing happening?

I think background radiation and radio stations, waste EM, and more is a beast, and there's a huge difference between getting something to fire in a mouse or beetle, and extending that to gene therapy so complex and subtle that it allows for large-scale control.

I'd add, you'd have a LOT of fatalities if you do that, and...

...You know what? Just no. I hate to say a flat no, but in this case... no.
 
Channelrhodopsins respond to light because they contain a chromophore molecule (retinal) that can switch between two different shapes. The activation energy, the amount of energy that it takes to switch the chromophore between these two states, is about 240 kJ/mol, which corresponds to the energy of a blue photon (480nm). If we wanted to engineer a rhodopsin to be sensitive to radio frequencies, what activation energy would we want our chromophore to have? Well, let's take the frequency of one of my favorite radio stations 106.7 MHz (let's round to 100 MHz), which would correspond to a wavelength of about 3 m, and an energy of about 0.04 kJ/mol. Therefore, the activation energy required to change the shape of the chromophore molecule would have to be about 0.04 kJ/mol.

Do you see the problem? At human body temperature (37oC, 310K), the amount of thermal energy available is about 2.6 kJ/mol. This means that thermal energy alone will be enough to activate our hypothetical radio-sensitive rhodopsin! The protein would not actually be able to sense radio waves because it would always be on regardless of whether or not radio waves were present.

If you look at calculations like these, you'll see that it is not an accident that animal vision is limited to a small range of the EM spectrum ranging from the near IR to the near UV. It is determined, rather, by the laws of physics. At frequencies significantly below the visible region, you get to the point where thermal energy becomes more energetic than the photons and a chromophore would not be able to distinguish thermal energy from the absorption of photons. At frequencies significantly above the visible region, you get into the range of ionizing radiation, photons so energetic that their energies are comparable to the activation energies for breaking chemical bonds.
 
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