But today, I thought I'd share with you the joy of having my own restriction endonuclease named after me. Well, not exactly named after me, but it has the same initials as me - elevating me to cool status. What restriction enzyme do I share my initials with???
Answer: MscI
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If you're not aware, restriction enzymes are like scissors, but in chemical form. They take long strings of DNA and cut at sequence specific sites. For example, if you had the DNA sequence 5'-GATCTAGGAATTCTCTAG-3' then at that bold spot, the restriction enzyme EcoRI could cut that DNA, separating it into two pieces. Cool, huh? But remember, DNA is double stranded; so when it cuts, it looks like this:
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These enzymes were originally discovered in bacteria as a defense mechanism against foreign pieces of DNA from invading viruses and other sources. Remember, if bacteria exchange genetic information then they're having a form of sex and they don't want to do that with just anything. There are many of these enzymes out there that have been discovered, and each one cuts only at its sequence specific site. Interestingly, all restriction enzyme sites are palindromes, or they are the same sequence forward as they are backwards. So using our host of enzymes, we can cut and paste our way into the genetics of the future.
I wonder what properties I share with my restriction enzyme ... ? According to New England Biolabs I work at 75% in Buffers 1, 2, and 3, and at 100% in Buffer 4. I'm not sensitive to methylation or CpG methylation, but with dcm methylation I am blocked by overlapping. You can heat inactivate me at 65 degrees Celsius for 20 minutes but I work optimally at 37 degrees Celsius. I'm an isochizomer of BalI and if I'm not working well, just give me a little more KCl and I'll get the job done.
Does that turn you on?