Team:DTU-Denmark-2/Project/Other assembly systems

From 2011.igem.org

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<a name="The way it's done"></a><h4><b>The way it's done</b></h3><br>
<a name="The way it's done"></a><h4><b>The way it's done</b></h3><br>
The Standard assembly uses the restrictionsites of four restriction enzymes; EcoRI and XbaI on the upstream and SpeI and Pst downstream of the BioBrick part on the vector. This sites are used to cut a DNA fragment (BioBrick) out of the plasmid and open the second and receiving plasmid. The resulting insert and open vector must be purified so unwanted and unspecified parts can be removed before the recombination of the insert and the cut plasmid. <br>The inset and cut plasmid are mixed and under the right conditions the sticky ends from the specified restriction will re-ligate, resulting in a vector containing both parts. The vector can now be transformed into E-coli. For good results it's important that the starting plamids only contain one restriction site for the used enzymes, others must be eliminated. <br>
The Standard assembly uses the restrictionsites of four restriction enzymes; EcoRI and XbaI on the upstream and SpeI and Pst downstream of the BioBrick part on the vector. This sites are used to cut a DNA fragment (BioBrick) out of the plasmid and open the second and receiving plasmid. The resulting insert and open vector must be purified so unwanted and unspecified parts can be removed before the recombination of the insert and the cut plasmid. <br>The inset and cut plasmid are mixed and under the right conditions the sticky ends from the specified restriction will re-ligate, resulting in a vector containing both parts. The vector can now be transformed into E-coli. For good results it's important that the starting plamids only contain one restriction site for the used enzymes, others must be eliminated. <br>
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Among disadvantages is the need for restriction digestions, ligations and DNA extraction from a gel before the assemling can be realized.
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<b>Difference between Plug'n Play assembly and Standard Assembly</b>
 +
The biggest disadvantages for the Standard assembly is the need for restriction digestions, ligations and the need for site-directed mutagenesis if more restriction sites are available on the plasmid. The limitation in only assembling two parts at the time, makes the Standard assembly much more time consuming. And last the scars made by the assembling, make it impossible to create fusion proteins by the Standard assembly.
   
   
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<a name="The way it's done"></a><h4><b>The way it's done</b></h3><br>
<a name="The way it's done"></a><h4><b>The way it's done</b></h3><br>
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The isothermal One-step The 5´-T5 exonuclease removes the bases from the 5'-end of double strained DNA molecule, leaving a recess in the DNA. The ssDNA overhang is used to assemble the DNA fragments.<br> The T5 exonuclease are inactivated during the incubation at 50ºC. Phusion polymerase and Taq ligase fills the gaps of the annealed complementary ssDNA overhangs and seals the nicks in the end, leaving a joined DNA molecules.  
+
The isothermal One-step The 5´-T5 exonuclease removes the bases from the 5'-end of double strained DNA molecule, leaving a recess in the DNA. The ssDNA overhang is used to assemble the DNA fragments.<br> The T5 exonuclease are inactivated during the incubation at 50ºC. Phusion polymerase and Taq ligase fills the gaps of the annealed complementary ssDNA overhangs and seals the nicks in the end, leaving a joined DNA molecules, ready for transformation. <br>
 +
<b>Difference between Plug'n Play assembly and Gibson Assembly</b>
 +
One of the disadvantages by the Gibson assembly is that the primers for the assembly is more expensive.
<br><br>
<br><br>
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The Gateway Assambly can clone up to 4 DNA fragments into one vector with by flanking the PCR products with specific att sites, and further directed recombination into the vector. The idea with Gateway assembly is that it is executed in the same way whether you join two or four DNA fragments. Depending on the number of fragments specific att sites are attached, always starting with attB1 and ending with attB2. The att sites only differ in a few bases.  <br>
The Gateway Assambly can clone up to 4 DNA fragments into one vector with by flanking the PCR products with specific att sites, and further directed recombination into the vector. The idea with Gateway assembly is that it is executed in the same way whether you join two or four DNA fragments. Depending on the number of fragments specific att sites are attached, always starting with attB1 and ending with attB2. The att sites only differ in a few bases.  <br>
First PCR fragments with the appropriate att sites and orientation has to be constructed as shown in <b>figure ??</b>  
First PCR fragments with the appropriate att sites and orientation has to be constructed as shown in <b>figure ??</b>  
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and then assembled with a Entry Clone, containing the respective att sites. The Entry Clones are mixed together with the appropriate destination vector by a LR clonase reaction. The resulting expression clone is then ready for tranformation and functional assays.  
+
and then assembled with a Entry Clone, containing the respective att sites. The Entry Clones are mixed together with the appropriate destination vector by a LR clonase reaction. The resulting expression clone is then ready for tranformation and functional assays. <br>
 +
<b>Difference between Plug'n Play assembly and Standard Assembly</b>
 +
 
<br><br>
<br><br>
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<a name="The way it's done"></a><h4><b>The way it's done</b></h3><br>
<a name="The way it's done"></a><h4><b>The way it's done</b></h3><br>
The assembled parts can either be in two plasmids or generated by PCR. The Methode uses the restriction sites of  EcoRI, SpeI, Xbal and Pst to flanke the Biobricks and destination vector. The difference with 3A and standard assembly is also that 3A uses three way ligation instead of only two. Digestion of the two parts and the destination plasmid are done so sticky ends are compatible with the wanted assembly of the vector. The restriction digest and ligation has to be executed in two separate steps.<br> After transformation into competent E.coli cells, the selection can be done by positive or negative selection.  
The assembled parts can either be in two plasmids or generated by PCR. The Methode uses the restriction sites of  EcoRI, SpeI, Xbal and Pst to flanke the Biobricks and destination vector. The difference with 3A and standard assembly is also that 3A uses three way ligation instead of only two. Digestion of the two parts and the destination plasmid are done so sticky ends are compatible with the wanted assembly of the vector. The restriction digest and ligation has to be executed in two separate steps.<br> After transformation into competent E.coli cells, the selection can be done by positive or negative selection.  
-
One of the disadvantages with 3A assembly is the need for plasmids to contain three different antiobiotic cassettes, beside the use of restriction digest and ligation.
+
<b>Difference between Plug'n Play assembly and 3A assembly</b>
 +
One of the disadvantages with 3A assembly is the need for plasmids to contain three different antiobiotic cassettes, beside the use of restriction digest and ligation leaving a scar on the plasmid. This method is also only capable in combining two parts at a time.  
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<ul>

Revision as of 21:36, 11 September 2011



Other assembly systems



Standard BioBrick Assembly


the Standard Assembly of BioBricks was first suggested by Tom Knight, and has subsequently been modified by other scientist to overcome hurdles in the Standard Assembly. In the Standard assembly their can only be assembled two parts in each cycle. The assembly system depends on two was ligase, meaning that the one assembles part has to be in the destination vector from the beginning.

The way it's done


The Standard assembly uses the restrictionsites of four restriction enzymes; EcoRI and XbaI on the upstream and SpeI and Pst downstream of the BioBrick part on the vector. This sites are used to cut a DNA fragment (BioBrick) out of the plasmid and open the second and receiving plasmid. The resulting insert and open vector must be purified so unwanted and unspecified parts can be removed before the recombination of the insert and the cut plasmid.
The inset and cut plasmid are mixed and under the right conditions the sticky ends from the specified restriction will re-ligate, resulting in a vector containing both parts. The vector can now be transformed into E-coli. For good results it's important that the starting plamids only contain one restriction site for the used enzymes, others must be eliminated.
Difference between Plug'n Play assembly and Standard Assembly The biggest disadvantages for the Standard assembly is the need for restriction digestions, ligations and the need for site-directed mutagenesis if more restriction sites are available on the plasmid. The limitation in only assembling two parts at the time, makes the Standard assembly much more time consuming. And last the scars made by the assembling, make it impossible to create fusion proteins by the Standard assembly.

Gibson Assembly


Gibson Assembly is an isothermal, single-reaction method for assembling multiple overlapping DNA molecules. The method was developed by Daniel G. Gibson at the J. Craig Venter Institute in 2009.
The assembly system employs 5´-T5 exonuclease, Phusion DNA polymerase, and Taq lig. Gibson can be used to assemble both ssDNA and dsDNA fragments. This methode makes it possible to join DNA molecules there are as large as 583kb and clone joined products in ''E. coli'' with a length up to 300kb. Among the advantages is that it takes the same amount of time to ligate n DNA fragments than two.



 

The way it's done


The isothermal One-step The 5´-T5 exonuclease removes the bases from the 5'-end of double strained DNA molecule, leaving a recess in the DNA. The ssDNA overhang is used to assemble the DNA fragments.
The T5 exonuclease are inactivated during the incubation at 50ºC. Phusion polymerase and Taq ligase fills the gaps of the annealed complementary ssDNA overhangs and seals the nicks in the end, leaving a joined DNA molecules, ready for transformation.
Difference between Plug'n Play assembly and Gibson Assembly One of the disadvantages by the Gibson assembly is that the primers for the assembly is more expensive.

Gateway assembly


MultiSite Gateway Assembly enables the assembly of multiple DNA fragments by utilizing site-specific recombination, and are provided by Invitrogen.Recombination is a efficient and quick way to assemble biobricks and are widely used. Invitrogen have designed standalized and simplified the technique in their Gateway Cloning.
Gateway Assembly uses two different bacteriophage recombination enzymes to assemble tje destination vector with the Entry clones. The process is extremely robust and furthermore overcome the steps by traditional restriction cloning.


The way it's done


The Gateway Assambly can clone up to 4 DNA fragments into one vector with by flanking the PCR products with specific att sites, and further directed recombination into the vector. The idea with Gateway assembly is that it is executed in the same way whether you join two or four DNA fragments. Depending on the number of fragments specific att sites are attached, always starting with attB1 and ending with attB2. The att sites only differ in a few bases.
First PCR fragments with the appropriate att sites and orientation has to be constructed as shown in figure ?? and then assembled with a Entry Clone, containing the respective att sites. The Entry Clones are mixed together with the appropriate destination vector by a LR clonase reaction. The resulting expression clone is then ready for tranformation and functional assays.
Difference between Plug'n Play assembly and Standard Assembly

In fusion


In-fusion BioBrick assembly are a methode for assembling of two or many Biobricks, provided by Clontech. The assembly system can be semi-standarlized by simple primer design rules, minimizing the time used on planning the assembly reactions.

The way it's done


The PCR fragments are assembled with the use of at least 15pb homology on both ends. The forward primer on the first PCR fragments must have homologes to the reverse primer of the second PCR fragment and so forth on every part of the BioBricks. Afterwards the PCR fragments can be fused into a pre-engineered vector by creation of single-stranded regions made by the In-fusion enzyme.
The reaction is fast an efficient but one of the disadvantages is that the suppliers are mote expensive, costume primers and occasionally mutations.

Sandwich



3A


The 3A assembly, like the Standard assembly, only join 2 BioBrick parts. To select the correct assemblies, the method uses the function of antibiotics which minimize time compared to gel purification.

The way it's done


The assembled parts can either be in two plasmids or generated by PCR. The Methode uses the restriction sites of EcoRI, SpeI, Xbal and Pst to flanke the Biobricks and destination vector. The difference with 3A and standard assembly is also that 3A uses three way ligation instead of only two. Digestion of the two parts and the destination plasmid are done so sticky ends are compatible with the wanted assembly of the vector. The restriction digest and ligation has to be executed in two separate steps.
After transformation into competent E.coli cells, the selection can be done by positive or negative selection. Difference between Plug'n Play assembly and 3A assembly One of the disadvantages with 3A assembly is the need for plasmids to contain three different antiobiotic cassettes, beside the use of restriction digest and ligation leaving a scar on the plasmid. This method is also only capable in combining two parts at a time.

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