Template:Team:Bonn:NetworkData

From 2013.igem.org

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content.titleLong = "Protein regulation mechanisms";  
content.titleLong = "Protein regulation mechanisms";  
content.summary= "We compare different regulation systems, focused on advantages and disadvanteges for scienticific use";
content.summary= "We compare different regulation systems, focused on advantages and disadvanteges for scienticific use";
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content.text= "To understand the role of a specific gene or DNA region is one of the big challenges in modern research. Our system, which allows the  
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content.text= "To understand the role of a specific gene or DNA region is one of the big challenges in modern research. Our system, which allows the <b>fast</b> and <b>convenient</b> elimination of defined proteins, is a new improved technique, with many advantages. The following table compares methods, advantages and disadvantages of several popular regulation methods.</br></br><table><tr><td><i>Regulation system</i></td><td><i>Approach of regulation</i></td><td><i>Activating / repressing</i></td><td><i>advantage</i></td><td><i>disadvantage</i></td></tr><tr><td><b>Knock-In</b></td><td>Insert of DNA</td><td>activating</td><td>gain of function; high difference of activity</td><td>No ON/OFF system</td></tr><tr><td><b>Knock-Out</b></td><td>Deletion of DNA</td><td>desactivating</td><td>0% Protein in organism</td><td>no ON/OFF system</td></tr><tr><td><b>Knock-Down<b></td><td>Inhibition of RNA</td><td>Repressing</td><td>inducible</td><td>Eypensive; small activity difference</td></tr><tr><td><b>Riboswitches</b></td><td>mRNA structure; Transcription & Translation</td><td>Activating/ repressing/ degradation</td><td>Multiple aproaches and effects</td><td>harder to modulate<td></tr><tr><td><b>Zymogen-like</b></td><td>Protein structure</td><td>Activating</td><td>Inducible</td><td>No deactivation</td></tr><tr><td><b>Operon</b></td><td>Transcription</td><td>Inductive (substrate)/ repressing (product)</td><td>Self-regulating in organisms</td><td>Not usable for every protein</td></tr><tr><td><b>TALEs</b></td><td>Transcription</td><td>Both</td><td>Can bind several effectors</td><td>Very specific</td></tr><tr><td><b>Zinc finger</b><td>Transcription</td><td>Both</td><td>Can bind several effectors</td><td>Very specific</td></tr><tr><td><b>Direct regulation</b></td><td>Protein affinity</td><td>Both</td><td>Very fast</td><td>Too specific for easy, general use</td></tr><tr><td><b>ClpXP protease system</b></td><td>Protein degradation</td><td>&quot;Repressing&quot;</td><td>Very fast & transferable</td><td> No obvious disadvantage</td></tr></table></break></br>After the comparison of all the different Protein regulation mechanisms, our team decided to make use of a protein degradation system. The reason was that we wanted to create a system that has an immediate effect and can be used to investigate functions of every protein.";
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<b>fast</b> and <b>convenient</b> elimination of defined proteins, is a new improved technique, with many advantages. The following table compares methods,  
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advantages and disadvantages of several popular regulation methods.</br></br><table><tr><td><i>Regulation system</i></td><td><i>Approach of  
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regulation</i></td><td><i>Activating / repressing</i></td><td><i>advantage</i></td><td><i>disadvantage</i></td></tr><tr><td><b>Knock-In</b></td><td>Insert of  
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DNA</td><td>activating</td><td>gain of function; high difference of activity</td><td>No ON/OFF system</td></tr><tr><td><b>Knock-Out</b></td><td>Deletion of  
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DNA</td><td>desactivating</td><td>0% Protein in organism</td><td>no ON/OFF system</td></tr><tr><td><b>Knock-Down<b></td><td>Inhibition of  
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RNA</td><td>Repressing</td><td>inducible</td><td>Eypensive; small activity difference</td></tr><tr><td><b>Riboswitches</b></td><td>mRNA structure;  
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Transcription & Translation</td><td>Activating/ repressing/ degradation</td><td>Multiple aproaches and effects</td><td>harder to  
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modulate<td></tr><tr><td><b>Zymogen-like</b></td><td>Protein structure</td><td>Activating</td><td>Inducible</td><td>No  
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deactivation</td></tr><tr><td><b>Operon</b></td><td>Transcription</td><td>Inductive (substrate)/ repressing (product)</td><td>Self-regulating in  
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organisms</td><td>Not usable for every protein</td></tr><tr><td><b>TALEs</b></td><td>Transcription</td><td>Both</td><td>Can bind several  
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effectors</td><td>Very specific</td></tr><tr><td><b>Zinc finger</b><td>Transcription</td><td>Both</td><td>Can bind several effectors</td><td>Very  
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specific</td></tr><tr><td><b>Direct regulation</b></td><td>Protein affinity</td><td>Both</td><td>Very fast</td><td>Too specific for easy, general  
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use</td></tr><tr><td><b>ClpXP protease system</b></td><td>Protein degradation</td><td>&quot;Repressing&quot;</td><td>Very fast & transferable</td><td> No  
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obvious disadvantage</td></tr></table></break></br>After the comparison of all the different Protein regulation mechanisms, our team decided to make use of a  
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protein degradation system. The reason was that we wanted to create a system that has an immediate effect and can be used to investigate functions of every  
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protein.";
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content.type="Background";  
content.type="Background";  
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break;

Revision as of 20:32, 1 October 2013