Difference between revisions of "Part:BBa K3588003"
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<partinfo>BBa_K3588003 short</partinfo> | <partinfo>BBa_K3588003 short</partinfo> | ||
| − | The mutant enzyme of part ([[part:BBa_K3588001]]). It is able to breakdown cocaine, as well as benzoylecogonine cocaethylene, through hydrolysis into benzoate and ecgonine methyl ester. With a dramatically increased <i>in vitro</i> half life from the wildtype enzyme it is currently in phase II trials as a cocaine overdose treatment,<ref>https://pubs.acs.org/doi/abs/10.1021/cb500257s</ref> though in our project we were intending to use it to breakdown cocaine in the sewers. | + | The mutant enzyme of part ([[part:BBa_K3588001]]). It is able to breakdown cocaine, as well as benzoylecogonine and cocaethylene, through hydrolysis into benzoate and ecgonine methyl ester. With a dramatically increased <i>in vitro</i> half life from the wildtype enzyme it is currently in phase II trials as a cocaine overdose treatment,<ref>https://pubs.acs.org/doi/abs/10.1021/cb500257s</ref> though in our project we were intending to use it to breakdown cocaine in the sewers. |
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===Function=== | ===Function=== | ||
The enzyme was designed in order to deal with the problem of drug overdosing, by administering an enzyme with a high catalysis rate into the bloodstream of patients who are overdosing, the effects can be rapidly reduced, however the problem posed by the usage of naturally occurring CocE is its lack of thermal stability (half life at 37°C = ~12mins), so by changing the bonding of the protein chain a more thermally stable version of the enzyme was created, thereby increasing its potential for <i>in vivo</i> usage, thus the current trials it is undergoing. | The enzyme was designed in order to deal with the problem of drug overdosing, by administering an enzyme with a high catalysis rate into the bloodstream of patients who are overdosing, the effects can be rapidly reduced, however the problem posed by the usage of naturally occurring CocE is its lack of thermal stability (half life at 37°C = ~12mins), so by changing the bonding of the protein chain a more thermally stable version of the enzyme was created, thereby increasing its potential for <i>in vivo</i> usage, thus the current trials it is undergoing. | ||
| + | [[File:CocE Catalytic Activity.png|none|800px|thumb| The enzyme CocE catalyses the breakdown of cocaine into benzoate and ecgonine methyl ester <ref>http://dx.doi.org/10.1128/aem.66.3.904-908.2000</ref>]] | ||
===properties=== | ===properties=== | ||
Revision as of 15:18, 24 October 2020
Cocaine Esterase mutant enzyme (E172-173)
The mutant enzyme of part (part:BBa_K3588001). It is able to breakdown cocaine, as well as benzoylecogonine and cocaethylene, through hydrolysis into benzoate and ecgonine methyl ester. With a dramatically increased in vitro half life from the wildtype enzyme it is currently in phase II trials as a cocaine overdose treatment,[1] though in our project we were intending to use it to breakdown cocaine in the sewers.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BamHI site found at 1179
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
Function
The enzyme was designed in order to deal with the problem of drug overdosing, by administering an enzyme with a high catalysis rate into the bloodstream of patients who are overdosing, the effects can be rapidly reduced, however the problem posed by the usage of naturally occurring CocE is its lack of thermal stability (half life at 37°C = ~12mins), so by changing the bonding of the protein chain a more thermally stable version of the enzyme was created, thereby increasing its potential for in vivo usage, thus the current trials it is undergoing.
properties
Cocaine Substrate Kinetics
Kcat = 2600 min-1 KM = 2.9 μM
other details
half life (at 37°C) = ~ 6hrs
usage
- ↑ https://pubs.acs.org/doi/abs/10.1021/cb500257s
- ↑ http://dx.doi.org/10.1128/aem.66.3.904-908.2000