Radio activated rhodopsin-like protein?

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Discussion Overview

The discussion revolves around the hypothetical creation of a radio frequency-activated rhodopsin-like protein that could control brain cells in a manner similar to channelrhodopsins, which respond to light. Participants explore the feasibility and implications of such a concept, touching on genetic engineering, neuroscience, and the potential for large-scale control over populations.

Discussion Character

  • Exploratory
  • Debate/contested
  • Conceptual clarification

Main Points Raised

  • One participant proposes the idea of synthesizing a protein that responds to radio frequencies, suggesting it could allow for control over populations via viral transfection and radio transmitter towers.
  • Another participant challenges this idea, citing the complexities of gene therapy and the potential for fatalities, ultimately expressing strong skepticism about the feasibility of such control.
  • A third participant provides a technical analysis of the activation energy required for a hypothetical radio-sensitive rhodopsin, explaining that at human body temperature, thermal energy would exceed the energy from radio frequency photons, making it impossible for the protein to function as intended.
  • A fourth participant humorously suggests a connection between this concept and genetically engineered food, framing it as a basis for a fictional "Zombie apocalypse."

Areas of Agreement / Disagreement

Participants express differing views on the feasibility of creating a radio frequency-activated rhodopsin. While one participant is optimistic about the potential, others raise significant doubts and concerns, indicating that the discussion remains unresolved with multiple competing perspectives.

Contextual Notes

Limitations include the assumptions about the viability of genetic engineering and the specific conditions under which a radio-sensitive rhodopsin could function. The discussion also highlights the challenges posed by thermal energy in distinguishing between radio frequency signals and background thermal noise.

sammysoil
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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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I'm pulling my tinfoil hat out of storage. If you combine this thread with genetically engineered food, we have a new basis for the mechanism behind the coming Zombie apocalypse. Hypothetically speaking of course.
 

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