Team:SYSU-China/file/Project/Background.html

From 2014.igem.org

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<h1>Background</h1>
<h1>Background</h1>
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Protein is one of the most powerful gift created by nature. Artificial protein products have been broadly applied in scientific researches, pharmaceutical industry, new energy fields and etc. Though protein's composition have been well-studied, even till nowadays, acquiring protein with new function is a laborious task for human. The current method to engineer protein, such as ration design and directed evolution, is both inefficient and labor-intensive.
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Artificial protein products have been broadly applied in scientific researches, pharmaceutical industry, new energy fields, etc. Though being well-studied, even till nowadays, acquiring proteins with aimed new function is still a laborious task. The current method of engineering protein, such as ration design and directed evolution, is both inefficient and labor-intensive for involving manual operation all the steps.
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To overcome this dilemma, this year, by integrating the separated steps of traditional directed evolution, SYSU-China intends to build an Integrated Evolution Machine, a system enabling us to obtain desired new protein in a short time automatically.
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To overcome this dilemma, by integrating the separated steps of traditional directed evolution (Annotation see below) into life cycle of modified Enterobacteria phage M13 (Annotation see M13 part), SYSU-China intends to build Integrated Evolution Machine (IgEM), a system enabling us to obtain desired protein in a short time automatically.
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For the natural evolution process, inherent mutation provides the raw materials, then the natural selection drive the fittest dominating. In artificial evolution system, the selective force is manually chosen, directing the raw materials evolve to gain the expected function. However, for traditional directed evolution system, mutagenesis, selection and domination all need manual intervention, which makes the process slow and complicated.  
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In our system, the primitive protein coding sequence would evolve spontaneously as modified M13 phage infects the host and replicates itself. With the assistance of mutagenesis module (Link) in the engineered host, mutation could be rapidly introduced into the sequence. Different from the previous design (Liu DR et al., 2011), Bacterial Two-hybrid System (Link) provides the selective pressure in system, screening the protein trending with specific protein-protein interaction activity. As the gVIII deleted M13 phage is budding-deficient, the output from bacterial two-hybrid system renders the phage coding expected new protein advantage during evolution. Later, under the control of RNAT module (Link), phage carrying prospective protein coding sequence would be able to generate progeny and gradually become dominance.  
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In our system, therefore, in order to avoid laborious manipulation, the raw protein coding sequence is integrated into the genome of Enterobacteria phage M13, which enables the protein mutating spontaneously with the assistance of mutagenesis module in the engineered host. Different from the previous design(Liu DR et al., 2011), Bacterial Two-hybrid System provides the selective force in system, screening the protein with specific protein-protein interaction activity. Later, under the control of built-in RNAT module in host, phage carrying wanted protein sequence would be able to generate progeny and gradually become dominance.
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Traditional directed evolution
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<p>
<p>
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Artificial protein products have been broadly applied in scientific researches, pharmaceutical industry, new energy fields, etc. Though being well-studied, even till nowadays, acquiring proteins with aimed new function is still a laborious task. The current method of engineering protein, such as ration design and directed evolution, is both inefficient and labor-intensive for involving manual operation all the steps.
+
Traditionally, directed evolution system consists of three steps, mutagenesis, selection and domination (amplification?). Firstly mutagenesis, usually realized by error-prone PCR, generates a pool of candidate protein coding sequences. Then, using screening techniques, such as phage display and yeast-two-hybrid system, certain candidates with expected property would be selected out. Finally, isolated ideal mutant sequence could be amplified by PCR. As the selective pressure is manually chosen, after several rounds of screening, the raw materials would be directly evolved to gain the expected function. Apparently, all steps above need manual intervention, which makes the process slow and complicated.
</p>
</p>
-
<p>
 
-
To overcome this dilemma, by integrating the separated steps of traditional directed evolution (Annotation see below), SYSU-China intends to build an Integrated Evolution Machine (IgEM), a system enabling us to obtain desired new protein in a short time automatically.
 
-
</p>
 
-
 
-
<p>
 
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In our system, to avoid laborious manipulation, steps of directed evolution are integrated into life cycle of Enterobacteria phage M13 (Annotation see M13 part). In this way, with the assistance of mutagenesis module in the engineered host, primitive protein coding sequence could mutate spontaneously as the M13 phage infects and replicates. Different from the previous design (Liu DR et al., 2011), Bacterial Two-hybrid System provides the selective force in system, screening the protein with specific protein-protein interaction activity. Later, under the control of built-in RNAT module in host, phage carrying wanted protein sequence would be able to generate progeny and gradually become dominance.
 
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</p>
 
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<p>
 
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Annotation of Traditional directed evolution
 
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Traditionally, directed evolution system consists of three steps, mutagenesis, selection and domination (amplification?). Firstly mutagenesis, usually realized by error-prone PCR, generates a pool of candidate protein coding sequences. Then, using screening techniques, such as phage display and yeast-two-hybrid system, certain candidates with expected property would be selected out. Finally, isolated ideal mutant sequence could be amplified by PCR. As the selective force is manually chosen, after several rounds of screening, the raw materials would be directly evolved to gain the expected function. Apparently, all steps above need manual intervention, which makes the process slow and complicated.
 
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Revision as of 20:45, 17 October 2014

Background

Artificial protein products have been broadly applied in scientific researches, pharmaceutical industry, new energy fields, etc. Though being well-studied, even till nowadays, acquiring proteins with aimed new function is still a laborious task. The current method of engineering protein, such as ration design and directed evolution, is both inefficient and labor-intensive for involving manual operation all the steps.

To overcome this dilemma, by integrating the separated steps of traditional directed evolution (Annotation see below) into life cycle of modified Enterobacteria phage M13 (Annotation see M13 part), SYSU-China intends to build Integrated Evolution Machine (IgEM), a system enabling us to obtain desired protein in a short time automatically.

In our system, the primitive protein coding sequence would evolve spontaneously as modified M13 phage infects the host and replicates itself. With the assistance of mutagenesis module (Link) in the engineered host, mutation could be rapidly introduced into the sequence. Different from the previous design (Liu DR et al., 2011), Bacterial Two-hybrid System (Link) provides the selective pressure in system, screening the protein trending with specific protein-protein interaction activity. As the gVIII deleted M13 phage is budding-deficient, the output from bacterial two-hybrid system renders the phage coding expected new protein advantage during evolution. Later, under the control of RNAT module (Link), phage carrying prospective protein coding sequence would be able to generate progeny and gradually become dominance.

Traditional directed evolution

Traditionally, directed evolution system consists of three steps, mutagenesis, selection and domination (amplification?). Firstly mutagenesis, usually realized by error-prone PCR, generates a pool of candidate protein coding sequences. Then, using screening techniques, such as phage display and yeast-two-hybrid system, certain candidates with expected property would be selected out. Finally, isolated ideal mutant sequence could be amplified by PCR. As the selective pressure is manually chosen, after several rounds of screening, the raw materials would be directly evolved to gain the expected function. Apparently, all steps above need manual intervention, which makes the process slow and complicated.


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