Using the forth flotation technique to mass produce SARS-CoV-2 serum

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Discussion Overview

The discussion revolves around the potential application of froth flotation techniques for the mass production of SARS-CoV-2 serum, specifically focusing on the separation of spike proteins and their use in antibody production without the need for traditional host-based methods. Participants explore various methods, including in vitro immunization and molecularly imprinted polymers, while also addressing the feasibility of using micro bubbles in this context.

Discussion Character

  • Exploratory
  • Technical explanation
  • Debate/contested

Main Points Raised

  • One participant proposes using froth flotation to separate spike proteins from SARS-CoV-2 for serum production, questioning the ability of micro bubbles to hold proteins without bursting.
  • Another participant suggests that traditional methods, such as ammonium sulfate precipitation and affinity columns, may be more effective for isolating antibodies from serum.
  • A different participant mentions the possibility of creating antibodies without a host and expresses interest in alternative applications of froth flotation beyond metal processing.
  • In vitro immunization methods and bacterial production of antibody molecules are briefly mentioned as potential alternatives.
  • One participant corrects the terminology from "forth flotation" to "froth flotation," indicating a possible misunderstanding of the technique.
  • Another participant introduces the idea of using molecularly imprinted polymers for binding spike proteins, suggesting modifications to enhance their surfactant properties.
  • Several participants discuss their learning processes, emphasizing the importance of academic courses, lab work, and reading specialized literature.

Areas of Agreement / Disagreement

Participants express a range of ideas and methods, with no clear consensus on the best approach for producing SARS-CoV-2 serum. Multiple competing views remain regarding the effectiveness of froth flotation versus traditional methods and alternative techniques.

Contextual Notes

Some participants express uncertainty about the feasibility of using micro bubbles and the specifics of in vitro immunization methods. There are also unresolved questions regarding the modifications needed for spike proteins to function effectively in proposed techniques.

Who May Find This Useful

This discussion may be of interest to researchers and practitioners in biochemistry, immunology, and separation techniques, particularly those exploring innovative methods for antibody production and protein separation.

hagopbul
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TL;DR
as i remember the 1st layer of SARS-ncov -2 have some hydrophobic and hydrophilic properties could we use this properties to mass produce the serum
Hello All:

i remember (and saw ) that the SARS-ncov-2 layers have hydrophobic and hydrophilic properties

few weeks ago i was reading about forth flotation and it is a method to separate metals , but on low temperature could we use it to separate the spike protein and mix it with immune cells to create the needed serum against the SARS-ncov-2 without the need to inject and wait until the animal produce the needed serum ( antibodies)

the bubbles in this system will separate the needed proteins and all we have to do is mix the outcome with some immune cells and wait until they produce the needed antibody

is it possible for the surface tension of a micro bubble to be able to hold large numbers of proteins without bursting ? what books you recommend on for the subject ?

how we can create a micro bubble in a liquid without using some thing that damage a cell membrane for example is there a physical methods to create bubbles in a liquid ? any books on the subject ?

Best
Hagop

any one wants to work with me on the subject ?
 
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This (I am assuming you want to get antibodies out of serum from someone who has an immunity to cvoid-19, perhaps the antibodies in the mix that bind Covid-19 proteins) is probably better done by traditional methods.

Antibodies (general mix) can be isolated by an ammonium sulfate precipitation. This can be done fairly easily in large volume.

You can isolate only the antibodies binding the virus if you can put proteins from the virus on column beads (beads commercially available for binding proteins in a column), using an affinity column. Put your antibodies in solution, soak them in the column until they are bound to the virus proteins you have immobilized on the beads in the column, put a new solution in the column that causes the antibodies to elute (detach from the column and come out in the wash) where you can collect them.

This stuff is pretty standard.
 
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I was talking also about creating antibodies without a host

And inspecting if this method is good for application other than metal processing

Day 5 self quarantine that gives you a lot of ideas
 
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There are methods for in vitro immunization.

I think there are also methods to make antibody molecules in bacteria (based on some plasmid trick I think).
However, I am not very familiar with them.
 
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hagopbul said:
few weeks ago i was reading about forth flotation

Forth? Froth!
 
epenguin said:
Forth? Froth!
 
Why don’t you consider Molecularly Imprinted Polymers for this instead? I came up with a method to imprint bile salts onto the surface of small spheres of polyacrylate using emulsion polymerization. The bile salts were a stand in for steroids of interest like testosterone or something like cholesterol. I’d bet spike proteins would work as well with a little modification to turn them into a surfactant. Hmmmmm...
 
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Whatever you guys are talking about, how do you learn it?
 
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cwill53 said:
Whatever you guys are talking about, how do you learn it?
In my case, taking chemistry/biochem classes, working in labs doing some separation techniques, reading papers and books on specialized techniques I am interested in.
I used to have a book on physical basis of biochemical separation techniques. It would have been interesting to me even if it did not deal with something I wanted to do in the lab.
 
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  • #10
reading about forth flotation and physics , the ideas attacks me without a notice if i don't talk about it then i forget it , and now trying to induce a discussion here on the forums maybe some thing new will come from it
 

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