QMUL Science Alive: Protein expression and purification

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QMULOfficial

QMULOfficial

6 жыл бұрын

E. coli bacteria are a common host for the expression of recombinant proteins used in a wide range of applications. Plasmids are circular DNA constructs which may encode instructions for the synthesis of an engineered protein by the desired host cells. Following transformation and selection of bacterial colonies containing the plasmid, the recombinant protein is expressed and purified. Poly-histidine tagging and Nickel ion chromatography are commonly used to isolate large quantities of highly-purified target proteins. This video will demonstrate the procedures involved, including expression of a His-tagged recombinant protein in bacteria, purification of the protein using Nickel ion affinity chromatography, and analysis using SDS-PAGE. Protein expression and purification is presented by James Wright and directed by Rosemary Clyne.

Пікірлер: 57
@calebsawe8307
@calebsawe8307 2 жыл бұрын
James Wright is a good teacher. It was almost I was there with him. I can picture the entire process. He also gave details and principles behind why certain reagents are used. Awesome video. Would like it 100 times if I could.
@jannabee3314
@jannabee3314 5 жыл бұрын
Took me 8 weeks to successfully express a protein, it's pretty simple in theory but doesn't always work smoothly in the lab, great video though!
@intuitivealpha328
@intuitivealpha328 4 жыл бұрын
how difficult are somatropes?
@danjbro
@danjbro 3 жыл бұрын
That's the truth!
@rolfw2336
@rolfw2336 5 жыл бұрын
I appreciate the buffer compositions that you overlayed on the video.
@Teragarm
@Teragarm 3 жыл бұрын
Great video! and for everyone alarmed by him not wearing gloves, it's very normal in bacteriology research!
@itsmemadle756
@itsmemadle756 2 жыл бұрын
Really thank you for the explanation of such a complicated process in a simpler way
@robweishart
@robweishart 4 жыл бұрын
Thank you for that great introduction and clear explanation!
@winter4ever567
@winter4ever567 3 жыл бұрын
Great Video! James, where ever you are, I hope you're doing well. Cheers bud
@78rydwan
@78rydwan 5 жыл бұрын
Great job, wish you all the best with your research.
@ericwuluglayjr6060
@ericwuluglayjr6060 2 жыл бұрын
That is precisely what I was looking for, thanks once more.
@nels6991
@nels6991 4 жыл бұрын
Great Video Thank you! Does anyone have any good sources for how this is done at the large industrial scale?
@all_about_microbiology_
@all_about_microbiology_ 4 ай бұрын
Very Useful Video , Thanks for this 👍
@danielrodriguezaguilar3867
@danielrodriguezaguilar3867 3 жыл бұрын
Cómo me gustaría que mi laboratorio estuviera así de equipado u.u Excelente vídeo, me encantó :3
@afifahusna6561
@afifahusna6561 4 жыл бұрын
i clapped when i see a beautiful nice band u got after purification. nice video
@SaraMonicaLeonUlloa
@SaraMonicaLeonUlloa 7 ай бұрын
Thank you for this video! It's cool how you do this in a lab!
@naemibickmeier4013
@naemibickmeier4013 4 жыл бұрын
You just made my day. Thank you so much.
@Drukonosz
@Drukonosz 3 жыл бұрын
Nice material!
@Tepmodify
@Tepmodify Жыл бұрын
I like video. Interesting . good describe
@hesnayigit8840
@hesnayigit8840 2 жыл бұрын
Thank you very much, this was a very good show and tell for the students.
@Artas1984
@Artas1984 5 жыл бұрын
That plasmid is missing a marker needed for individual colonies separation by color: a screening marker, that is in the MCS region.
@nels6991
@nels6991 4 жыл бұрын
the screen is already done by inserting the antibiotic resistance gene. A color marker would only be needed if the plasmids were a mix of plasmids with the target sequence and plasmids without the target sequence.
@xima7140
@xima7140 3 жыл бұрын
Hi, can we store the supernatant obtained after sonication and centrifugation that has expressed proteins?
@drshinwarishinwari1253
@drshinwarishinwari1253 5 жыл бұрын
No gloves 😱
@shilpawaduwawara9529
@shilpawaduwawara9529 4 жыл бұрын
Yea!! Freaks me out! Good video except for that though.
@drshinwarishinwari1253
@drshinwarishinwari1253 4 жыл бұрын
Shilpa Waduwawara 😀
@nicolasalarcon7162
@nicolasalarcon7162 3 жыл бұрын
If you're working with microorganisms near to a flame. Its dangerous wear gloves. Also the flame sterilize very good the surroundings and usually the bacteria had a antibiotic resistence to keep it clean.
@musabiremaalexis4477
@musabiremaalexis4477 2 жыл бұрын
Hello,Thank you for the video
@SouravGhosh-pn7bl
@SouravGhosh-pn7bl 3 жыл бұрын
Do you also use any eukaryotic system for protein expression followed by purification than bacterial system?
@j.m.e.r8539
@j.m.e.r8539 4 жыл бұрын
Nice video and very well explication! Congrats!
@nels6991
@nels6991 4 жыл бұрын
Are these E. coli producing proteins by cytosolic production, Inclusion body formation, secretory production, or excretory production?
@mlearningplus5183
@mlearningplus5183 4 жыл бұрын
Could you please guide cloning techniques step by step
@DrGhosh
@DrGhosh 5 жыл бұрын
1) The optical density of the E.Coli culture during IPTG induction and IPTG concentration? 2)Too much Ni-beads for that volume of the supernatant, so probably there was nonspecific binding of other protein to the beads leads to the tiny bands in elution lane. 3)The safety issue while the use of glass beaker for sonication. 4) no sample loading for wash step as well as beads!!
@houtsereywatana7539
@houtsereywatana7539 2 жыл бұрын
thank you for explaining
@markh1652
@markh1652 2 жыл бұрын
thanks for sharing!
@ChompNom
@ChompNom 5 жыл бұрын
gloves?
@richardfever
@richardfever 5 жыл бұрын
Wubbywub the First thing that I noticed
@xima7140
@xima7140 3 жыл бұрын
Not needed
@qamarhennawi9137
@qamarhennawi9137 2 жыл бұрын
Thank you so much
@AinaSakeenah
@AinaSakeenah 3 жыл бұрын
Thank you
@AA-gl1dr
@AA-gl1dr 3 жыл бұрын
thank you so much!
@rumjhumtyagi2880
@rumjhumtyagi2880 5 жыл бұрын
if the protein isn't expressed, what does that indicate? what mistakes could I have made?
@Structuralbiology
@Structuralbiology 3 жыл бұрын
Inducer is not able to remove repressor or other reasons may be that your bacterial does not allow the expression of protein
@titi14fan
@titi14fan 5 жыл бұрын
Thank you; it was brilliant
@Sulbee
@Sulbee 2 жыл бұрын
How do you talk so fast :D I was watching this for exam prep, and I had to slow it down :D Thanks for this though :)
@ericwuluglayjr6060
@ericwuluglayjr6060 2 жыл бұрын
THANKS ALOT ❤
@mkcd3829
@mkcd3829 3 жыл бұрын
You’re the best
@tremeramcbean3719
@tremeramcbean3719 2 жыл бұрын
Why aren’t you weren’t gloves?
@fatimahayssam120
@fatimahayssam120 5 жыл бұрын
is it a cell biology lab or biochemistry?
@jannabee3314
@jannabee3314 5 жыл бұрын
It can be any sort of biological or chemistry lab, I did this exact same procedure in a Biotechnology lab which was part of a school of chemistry.
@anisnadyraahmadzifruddin6820
@anisnadyraahmadzifruddin6820 3 жыл бұрын
where's your glove tho.........
@adronung1892
@adronung1892 3 жыл бұрын
No gloves?
@johnhuang113
@johnhuang113 Жыл бұрын
not feeling good without the gloves
@alexlee6859
@alexlee6859 3 жыл бұрын
So uh, what's he cooking?
@danjbro
@danjbro 3 жыл бұрын
Gloves dude...gloves!
@runningcookiess
@runningcookiess 6 ай бұрын
It’s not safe to do experiments without gloves and goggles
@jonbuitbuitrago6867
@jonbuitbuitrago6867 5 жыл бұрын
Thanks for this lab work divulgation
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