Used for the Cambridge Science Festival to explain our Phage Display Technology
Пікірлер: 29
@carl-johanhorberg13996 жыл бұрын
Thanks! Finally an explanation that puts it into a functional context.
@veraltol1706 жыл бұрын
i have been in difficultes somme days to cleary understand this method. i was stressed but this video helped me a lot! Merci beaucoup aux auteurs;
@Biomeducated5 жыл бұрын
The fishing can be done in several ways, depending on the target of interest and how it can be recombinantly produced (or not). For instance, you can interrogate your library of phages for selection on solid phase (where the antigen is coated on a plate), or in solution (where the antigen is coupled to beads). If you're antigen is difficult to produce (for instance a GPCR), you could select in solution on recombinant CHO or HEK cells expressing the target (allowing proper folding of the target). Furthermore, selection strategies can be designed for diversity, or for affinity, all depending on the goal of the discovery strategy. Informative introductory video on Phage Display! Cheers
@yandongan13454 жыл бұрын
so useful,thank you
@danielgladish25023 жыл бұрын
Wow! Great explanation and super interesting technique! Very high throughput
@chrissun996010 жыл бұрын
Very clear description. But I am confused how people know the gene can be expressed as an antibody inside the phage.
@scottcampbell63906 жыл бұрын
The antibody is displayed on the phage coat, which is outside of the phage capsule. The phage structure is built by the host bacteria. If we insert the gene encoding the desired antibody inside the coding region for the phage coat, the antibody will be expressed on the coat when the host bacteria replicates the phage.
@pluvia135 жыл бұрын
@@scottcampbell6390 yeah so because we cannot rely on the bacterias ability to correctly fold an eukaryotic molecule one has to consider that this molecule could differ in structure from what would be achieved in an eukaryotic cell using the same gene right?
@daoyuzhang16484 жыл бұрын
This could be what was used to generate the 100x higher-binding-affinity ACE2 RBD in Covid-19. Such high binding affinity have never been found in nature for betacoronaviruses in general.
@belindashaw18476 жыл бұрын
Would this be useful to other protein expression platforms, say in plants such as tobacco? And if you wanted to make a unique antibody that you didn't have the antigen for how could you go about that...? Thanks for the video was very helpful :)
@amonoracheal91182 жыл бұрын
Thank you for making it clear for me:)
@Biomeducated5 жыл бұрын
Excellent explanation and animation! It's also used to 'fish' for Nanobodies! If you don't know what Nanobodies are, I made an introductory video on my channel. Great video, Charlie Abbott!
@lauraricarte79386 жыл бұрын
this is simply fantastic
@pavarinodu4 жыл бұрын
Wow! That's fascinating!
@oidualclaudi02 жыл бұрын
Is this an alternative for the use of animals like rabbits and mice to produce antibodies?
@paffnblunt5006 жыл бұрын
from where do we take the genes at the beginning?
@Biomeducated5 жыл бұрын
Well, you could trigger an immune response in mice by injecting a human target, then you isolate the B-cells from the mouse, and then you extract the RNA from those B-cells, and you got yourself a library :)
@sandybravo64928 жыл бұрын
just wanted to know if we call it phage antibody or antibody phage
@lujainkhasawneh20208 жыл бұрын
Very Nice !
@nunitchagucci30475 жыл бұрын
Love your video!
@Biomeducated5 жыл бұрын
Yes, clear and concise, isn't it!
@nunitchagucci30475 жыл бұрын
@@Biomeducated
@ViskayaNuebler795 жыл бұрын
I think you helped me understand a paper i neededt to read