Team:Austin Texas/kit

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The above results represent the "perfect" tRNA synthetase/tRNA pair: one that has 100% fidelity and 100% efficiency.  Actual synthetase/tRNA pairs will occasionally misincorporate an incorrect amino acid, and these pairs will not always be perfectly efficient at conducting every step in the process of reading through an amber codon.]]
The above results represent the "perfect" tRNA synthetase/tRNA pair: one that has 100% fidelity and 100% efficiency.  Actual synthetase/tRNA pairs will occasionally misincorporate an incorrect amino acid, and these pairs will not always be perfectly efficient at conducting every step in the process of reading through an amber codon.]]
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*''' A)''' In a cell containing pStG and pFRYC, the ribosome will translate the RFP reporter, linker, and sfGFP, producing red and green fluorescent proteins that result in visible yellow fluorescence (Figure 3A).  This happens because the reporter contains no amber codon, and thus does not require a ncAA synthetase/tRNA pair.
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*''' A)''' In a cell containing pStG and pFRYC, the ribosome will translate the RFP reporter, linker, and sfGFP, producing red and green fluorescent proteins that result in visible yellow fluorescence ('''Figure 3A''').  This happens because the reporter contains no amber codon, and thus does not require a ncAA synthetase/tRNA pair.
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*''' B)''' If a cell contained only pFRY, without pStG, then the ribosome will translate the RFP and terminate at the amber codon on the linker producing a red fluorescence (Figure 3B).  This occurs because without the pStG, the amber codon is not recoded to allow for ncAA incorporation.
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*''' B)''' If a cell contained only pFRY, without pStG, then the ribosome will translate the RFP and terminate at the amber codon on the linker producing a red fluorescence ('''Figure 3B''').  This occurs because without the pStG, the amber codon is not recoded to allow for ncAA incorporation.
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* '''C)''' In a cell containing pStG and pFRY, there are multiple possible outcomes, depending on what is present in the culture.  In the absence of ncAA, the ribosome will translate the RFP and terminate at the amber stop codon on the linker producing a red fluorescence (Figure 3C).  This occurs because while the codon has been recoded, there is no ncAA and without ncAA there can be no incorporation at the amber codon.
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* '''C)''' In a cell containing pStG and pFRY, there are multiple possible outcomes, depending on what is present in the culture.  In the absence of ncAA, the ribosome will translate the RFP and terminate at the amber stop codon on the linker producing a red fluorescence ('''Figure 3C''').  This occurs because while the codon has been recoded, there is no ncAA and without ncAA there can be no incorporation at the amber codon.
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*''' D)''' In a cell containing pStG and pFRY, there are multiple possible outcomes.  In the PRESENCE of ncAA, the ribosome will translate the RFP, then it incorporates the ncAA at the amber codon in the linker, and finally it proceeds to translate the downstream sfGFP reporter, producing a visible yellow fluorescence (Figure 3D).  This occurs because the synthetase found in pStG can covalently attach the ncAA to the tRNA gene present in pStG.  This "charged tRNA" is then present during translation, allowing incorporation of the ncAA into the reporter protein.
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*''' D)''' In a cell containing pStG and pFRY, there are multiple possible outcomes.  In the PRESENCE of ncAA, the ribosome will translate the RFP, then it incorporates the ncAA at the amber codon in the linker, and finally it proceeds to translate the downstream sfGFP reporter, producing a visible yellow fluorescence ('''Figure 3D''').  This occurs because the synthetase found in pStG can covalently attach the ncAA to the tRNA gene present in pStG.  This "charged tRNA" is then present during translation, allowing incorporation of the ncAA into the reporter protein.
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However, the above scenarios assume that the synthetase/tRNA pair function efficiently and with high fidelity. 
 
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*Actual synthetase/tRNA pairs sometimes have '''low fidelity''', leading to the incorporation of an incorrect amino acid.  This "misincorporation" means that such a synthetase/tRNA pair would not give results that mimic Figure 3C in the absence of ncAA.  Rather, in the absence of ncAA, such a pair would give results similar to Figure 3D, full expression of RFP and sfGFP.  High rates of misincorporation are equivalent to '''low fidelity''', and tRNA synthetases with low fidelity are not ideal.
 
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*Actual synthetase/tRNA pairs can also sometimes have '''low efficiency'''.  As these are artificially selected pairs, sometimes they do not function as well as natural synthetase/tRNA pairs.  In such a case, the amount of sfGFP translated in Figure 3D might be significantly lower than expected.  '''low efficiency''' is also not ideal as it may limit levels of protein expression.
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However, the above scenarios assume that the synthetase/tRNA pair functions perfectly.  Some of these systems are non-ideal because they have:
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*'''LOW FIDELITY:''' Actual synthetase/tRNA pairs sometimes have '''low fidelity''', leading to the incorporation of an incorrect amino acid.  This "misincorporation" means that such a synthetase/tRNA pair would not give results that mimic '''Figure 3C''' in the absence of ncAA.  Rather, in the absence of ncAA, such a pair would give results similar to '''Figure 3D''', full expression of RFP and sfGFP.  High rates of misincorporation are equivalent to '''low fidelity''', and tRNA synthetases with low fidelity are not ideal because they give a mixture of protein products with the normal and new amino acids at the recoded position.
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*'''LOW EFFICIENCY:''' Actual synthetase/tRNA pairs can also sometimes have '''low efficiency'''.  As these are artificially selected pairs, sometimes they do not function as well as natural synthetase/tRNA pairs.  In such a case, the amount of sfGFP translated in '''Figure 3D''' might be significantly lower than expected.  '''low efficiency''' is also not ideal as it may limit levels of protein expression.
<h2>Experimental Preparation</h2>
<h2>Experimental Preparation</h2>
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[[File:Alex and Foil-covered incubator.jpg|200px|thumb|right|Protection of light-sensitive ncAAs using a foil-wrapped incubator.]]  
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[[File:Alex and Foil-covered incubator.jpg|220px|thumb|right|Protection of light-sensitive ncAAs using a foil-wrapped incubator.]]  
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An ncAA synthetase/tRNA pair was cloned into pStG and transformed into pFRYC amberless ''E. coli'' and pFRY amberless ''E. coli''. Other necessary control strains include RFP amberless ''E. coli'' (RFP control), sfGFP amberless ''E. coli'' (GFP control), amberless ''E. coli'' (cell background control), and LB media supplemented with ncAA (media background control). An overnight culture of each strain was grown in LB with the appropriate antibiotics at 37ºC and 225rpm. 10 mL of media with the appropriate antibiotics was inoculated with 100 µL of overnight culture and allowed to grow in the same conditions until the culture density was ~0.2-0.3 OD<sub>600</sub>, or ~3 hours. The 10 mL culture was split between 4 different sterile test-tubes, 2 mL of culture per tube. The conditions of the four test tubes were as follows:  
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Each ncAA synthetase/tRNA pair to be tested was cloned into pStG and transformed into pFRYC amberless ''E. coli'' and pFRY amberless ''E. coli''. Other necessary control strains include RFP amberless ''E. coli'' (RFP control), sfGFP amberless ''E. coli'' (GFP control), amberless ''E. coli'' (cell background control), and LB media supplemented with ncAA (media background control). An overnight culture of each strain was grown in LB with the appropriate antibiotics at 37ºC and 225rpm. 10 mL of media with the appropriate antibiotics was inoculated with 100 µL of overnight culture and allowed to grow in the same conditions until the culture density was ~0.2-0.3 OD<sub>600</sub>, or ~3 hours. The 10 mL culture was split between 4 different sterile test-tubes, 2 mL of culture per tube. The conditions of the four test tubes were as follows:  
*-IPTG,-ncAA
*-IPTG,-ncAA
*-IPTG,+ncAA  
*-IPTG,+ncAA  
*+IPTG, -ncAA
*+IPTG, -ncAA
*+IPTG, +ncAA
*+IPTG, +ncAA
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If the cultures did not have IPTG or an ncAA, an equal volume of sterile deionized water was added in order to keep the volumes between cultures constant. Once the water, the IPTG, and the ncAA were added appropriately, the cultures were allowed to grow to ~0.5 OD<sub>600</sub>. 70 µL of each culture condition and control culture were added to a separate well in clear-bottom black 96-well plate for fluorescence and OD<sub>600</sub> readings using a plate reader.  
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If the cultures did not have IPTG or ncAA, an equal volume of sterile deionized water was added in order to keep the volumes between cultures constant. Once the water, the IPTG, and the ncAA were added appropriately, the cultures were allowed to grow to ~0.5 OD<sub>600</sub>. 70 µL of each culture condition and control culture were added to a separate well in clear-bottom black 96-well plate for fluorescence and OD<sub>600</sub> readings using a plate reader.  
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ncAA-specific concerns accounted for and should be noted. These include: light-sensitivity, oxidation, and interference with fluorescence readings. Certain ncAAs were protected from light due to their light-sensitive molecular structures such as [https://2014.igem.org/Team:Austin_Texas/kit#ncAA_Table ONBY and AzF]. These ncAAs were prepared in a dark room and wrapped in foil. All cultures were grown in a foil-wrapped incubator for consistency. Some ncAAs are more prone to oxidation, specifically <small>L</small>-DOPA. When oxidized, the solution turns black. To prevent oxidation, each ncAA was prepared the day of the test for consistency. By this method, the oxidation of <small>L</small>-DOPA did not occur quickly enough to have an effect on the data. Most ncAA solutions were transparent once prepared with the exception of 3-nitro-<small>L</small>-tyrosine. The yellow-orange tint of 3-nitro-<small>L</small>-tyrosine solution was accounted for by measuring the fluorescence of 1mM 3-nitro-<small>L</small>-tyrosine in media and subtracting any possible background fluorescence from culture fluorescence grown in 1mM 3-nitro-<small>L</small>-tyrosine.
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We accounted for several ncAA-specific concerns. These included: light-sensitivity, oxidation, and interference with fluorescence readings. Certain ncAAs were protected from light due to their light-sensitive molecular structures such as [https://2014.igem.org/Team:Austin_Texas/kit#ncAA_Table ONBY and AzF]. These ncAAs were prepared in a dark room and wrapped in foil. All cultures were grown in a foil-wrapped incubator for consistency. Some ncAAs are more prone to oxidation, specifically <small>L</small>-DOPA. When oxidized, the solution turns black. To prevent oxidation, each ncAA was prepared the day of the test for consistency. By this method, the oxidation of <small>L</small>-DOPA did not occur quickly enough to have an effect on the data. Most ncAA solutions were transparent once prepared with the exception of 3-nitro-<small>L</small>-tyrosine. The yellow-orange tint of 3-nitro-<small>L</small>-tyrosine solution was accounted for by measuring the fluorescence of 1mM 3-nitro-<small>L</small>-tyrosine in media and subtracting any possible background fluorescence from culture fluorescence grown in 1mM 3-nitro-<small>L</small>-tyrosine.
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GFP fluorescence was measured using: excitation - 480 nm, emission - 525 nm
GFP fluorescence was measured using: excitation - 480 nm, emission - 525 nm
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[[File:10-14-14 big experiment test tubes.png|650px|thumb|left| Preparation for the ncAA Kit Test]]  
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[[File:10-14-14 big experiment test tubes.png|450px|thumb|left| Preparation for the ncAA Kit Test]]  
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[[File:RFP-GFP Controls 10-14-15.png|200px|thumb|right| A picture showing culture with or without IPTG.  Without IPTG, there is no induction of GFP (left).  With IPTG, strong fluorescence is easily seen (right).]]
[[File:RFP-GFP Controls 10-14-15.png|200px|thumb|right| A picture showing culture with or without IPTG.  Without IPTG, there is no induction of GFP (left).  With IPTG, strong fluorescence is easily seen (right).]]
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<h1>Results and Data</h1>
<h1>Results and Data</h1>
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The full list of ncAAs and their tRNA synthetase/tRNA pairs can be found in the [https://2014.igem.org/Team:Austin_Texas/kit#ncAA_Table tables at the bottom of this page].  These table include a plethora of information relevant for performing the experiments with each amino acid as well as sequencing data for each synthetase used.
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The full list of ncAAs and their tRNA synthetase/tRNA pairs can be found in the [https://2014.igem.org/Team:Austin_Texas/kit#ncAA_Table tables at the bottom of this page].  These table include a plethora of information relevant for performing the experiments with each amino acid as well as DNA sequencing data for each synthetase used.
<h2>Fidelity of Incorporation</h2>
<h2>Fidelity of Incorporation</h2>
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We wanted to test whether the ncAA synthetase/tRNA pairs would incorporate anything besides their amino acid at the amber stop codon (UAG), and that they would in fact incorporate their specific ncAA if it was present. This is essentially the fidelity of each ncAA sythetase/tRNA pair.
We wanted to test whether the ncAA synthetase/tRNA pairs would incorporate anything besides their amino acid at the amber stop codon (UAG), and that they would in fact incorporate their specific ncAA if it was present. This is essentially the fidelity of each ncAA sythetase/tRNA pair.
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Fidelity was measured by comparing the production of GFP in cultures containing pStG/pFRY with or without ncAA. In the absence of a ncAA only RFP should be translated, as translation is expected to halt between RFP and GFP at the amber codon on the linker sequence in pFRY. Alternatively, if the corresponding ncAA for pStG is present or if the synthetase/tRNA pair has low fidelity and can misincorporate a different amino acid, translation should continue through the UAG. In this case, RFP and GFP should both be translated. We also tested pStG/pFRYC strains in (+/-) ncAA conditions as a control for what effect the ncAA has on the fluorescence or growth of the cells. These strains should express RFP and GFP in all conditions since pFRYC does not have an amber codon in the linker (Figure 2).  However, if the presence of ncAA affects cell growth or fluorescence activity, we will need these controls to determine the extent of the effect.
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Fidelity was measured by comparing the production of GFP in cultures containing pStG/pFRY with or without ncAA. In the absence of a ncAA only RFP should be translated, as translation is expected to halt between RFP and GFP at the amber codon on the linker sequence in pFRY. Alternatively, if the corresponding ncAA for pStG is present or if the synthetase/tRNA pair has low fidelity and can misincorporate a different amino acid, translation should continue through the UAG. In this case, RFP and GFP should both be translated. We also tested pStG/pFRYC strains in (+/-) ncAA conditions as a control for what effect the ncAA has on the fluorescence or growth of the cells. These strains should express RFP and GFP in all conditions since pFRYC does not have an amber codon in the linker ('''Figure 2''').  However, if the presence of ncAA affects cell growth or fluorescence activity, we will need these controls to determine the extent of the effect.
To determine the change in GFP fluorescence when the ncAA was present, we first had to calculate how much GFP was expressed relative to the RFP, which would give an upper estimate of how much GFP could theoretically be expressed. We first divided both the GFP and RFP levels by the OD<sub>600</sub> of the culture in order to get the per cell fluorescence levels. We then normalized the GFP fluorescence for one culture to its RFP fluorescence so that we could compare the GFP fluorescence levels between cultures. The normalized GFP values were then compared between cultures grown in the presence of ncAA and cultures grown in the absence of ncAA, which would indicate how the level of GFP fluorescence changes when the ncAA is present.
To determine the change in GFP fluorescence when the ncAA was present, we first had to calculate how much GFP was expressed relative to the RFP, which would give an upper estimate of how much GFP could theoretically be expressed. We first divided both the GFP and RFP levels by the OD<sub>600</sub> of the culture in order to get the per cell fluorescence levels. We then normalized the GFP fluorescence for one culture to its RFP fluorescence so that we could compare the GFP fluorescence levels between cultures. The normalized GFP values were then compared between cultures grown in the presence of ncAA and cultures grown in the absence of ncAA, which would indicate how the level of GFP fluorescence changes when the ncAA is present.
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When these values were graphed (Figure 4), some synthetase/tRNA pairs such as 4-azido-<small>L</small>-phenylalanine (AzF), 3-nitro-<small>L</small>-tyrosine, 3-iodo-<small>L</small>-tyrosine, and ''o''-(2-nitrobenzyl)-<small>L</small>-tyrosine (ONBY) resulted in higher GFP fluorescence in the presence of ncAA than in the absence of ncAA, which suggests that those synthetases only incorporated an amino acid if their specific amino acid was present, meaning that they have a high fidelity. However, the other synthetase/tRNA pairs (3-amino-<small>L</small>-tyrosine, <small>L</small>-DOPA, and 4-cyano-<small>L</small>-phenylalanine (CNF)) did not show a difference in GFP fluorescence normalized to RFP fluorescence dependent on the presence of ncAA, indicating that these pairs incorporated other amino acids at the amber codon when their specific ncAA was not present (and perhaps even when it was), and thus have a low fidelity.
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When these values were graphed ('''Figure 4'''), some synthetase/tRNA pairs such as 4-azido-<small>L</small>-phenylalanine (AzF), 3-nitro-<small>L</small>-tyrosine, 3-iodo-<small>L</small>-tyrosine, and ''o''-(2-nitrobenzyl)-<small>L</small>-tyrosine (ONBY) resulted in higher GFP fluorescence in the presence of ncAA than in the absence of ncAA, which suggests that those synthetases only incorporated an amino acid if their specific amino acid was present, meaning that they have a high fidelity. However, the other synthetase/tRNA pairs (3-amino-<small>L</small>-tyrosine, <small>L</small>-DOPA, and 4-cyano-<small>L</small>-phenylalanine (CNF)) did not show a difference in GFP fluorescence normalized to RFP fluorescence dependent on the presence of ncAA, indicating that these pairs incorporated other amino acids at the amber codon when their specific ncAA was not present (and perhaps even when it was), and thus have a low fidelity.
<h2>Synthetase Efficiency</h2>
<h2>Synthetase Efficiency</h2>
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Another measure of quality for these ncAA synthetase/tRNA pairs is how efficiently they charge their ncAA, ultimately resulting in incorporation of the ncAA in our reporter protein. An inefficient synthetase/tRNA pair will yield incorporation of their ncAA only a fraction of the time, even when their ncAA is present. Our system can be used to measure this level of efficiency, though it does not indicate why a particular synthetase is efficient or inefficient. By comparing the level of GFP fluorescence to the normalized level of RFP fluorescence when the amino acid is present, we can see how efficient the synthetase is. In essence, if the normalized fluorescence of GFP relative to RFP is close to 100% (if the GFP is expressed roughly 100% of the time that RFP is expressed), then the synthetase is very efficient. On the other side, if say the normalized fluorescence of GFP relative to RFP is closer to 10%, then the synthetase would not be very efficient, because even when the ncAA was there, it only incorporated it at the amber codon about 10% of the time.
Another measure of quality for these ncAA synthetase/tRNA pairs is how efficiently they charge their ncAA, ultimately resulting in incorporation of the ncAA in our reporter protein. An inefficient synthetase/tRNA pair will yield incorporation of their ncAA only a fraction of the time, even when their ncAA is present. Our system can be used to measure this level of efficiency, though it does not indicate why a particular synthetase is efficient or inefficient. By comparing the level of GFP fluorescence to the normalized level of RFP fluorescence when the amino acid is present, we can see how efficient the synthetase is. In essence, if the normalized fluorescence of GFP relative to RFP is close to 100% (if the GFP is expressed roughly 100% of the time that RFP is expressed), then the synthetase is very efficient. On the other side, if say the normalized fluorescence of GFP relative to RFP is closer to 10%, then the synthetase would not be very efficient, because even when the ncAA was there, it only incorporated it at the amber codon about 10% of the time.
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For our results (Figure 4), two synthetase/tRNA pairs stood out as relatively inefficient: 3-nitrotyrosine and ONBY. Both of these synthetase/tRNA pairs showed a significantly smaller normalized GFP to RFP fluorescence when the ncAA was present with the pFRY construct. While both synthetase/tRNA pairs show a significant increase in normalized GFP to RFP fluorescence when the amino acid was present compared to when it was absent, which indicates a high fidelity, the actual GFP fluorescence relative to the RFP fluorescence was only around 50% for 3-nitrotyrosine and 20% for ONBY. These results suggest that, these synthetase/tRNA pairs do not always incorporate their ncAA at the amber stop codon.  It is important to note that this could partly result for ncAA-related toxicity, and such an effect was repeatedly observed for ONBY.
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For our results ('''Figure 4'''), two synthetase/tRNA pairs stood out as relatively inefficient: 3-nitro-<small>L</small>-tyrosine and ONBY. Both of these synthetase/tRNA pairs showed a significantly smaller normalized GFP to RFP fluorescence when the ncAA was present with the pFRY construct. While both synthetase/tRNA pairs show a significant increase in normalized GFP to RFP fluorescence when the amino acid was present compared to when it was absent, which indicates a high fidelity, the actual GFP fluorescence relative to the RFP fluorescence was only around 50% for 3-nitro-<small>L</small>-tyrosine and 20% for ONBY. These results suggest that these synthetase/tRNA pairs do not always efficiently incorporate their ncAA at an amber stop codon.  It is important to note that this could partly result from ncAA-related toxicity, and such an effect was repeatedly observed for ONBY.
<h2>Incorporation Value</h2>
<h2>Incorporation Value</h2>
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[[File:UT_Austin_2014_Kit_Incorporation_Value_Graph.png|600px|thumb|'''Figure 5.''' Incorporation values for each synthetase/tRNA pair.  Dash line equals an incorporation value of 1.  Values greater than 1 are desirable.  The GFP:RFP relative fluorescence values in the presence and absence of ncAA (see Figure 4) were used to calculate incorporation values.  Values were determined by dividing the GFP:RFP relative fluorescence in the presence of ncAA by the GFP:RFP relative fluorescence in the absence of ncAA. This value does not correct for ncAA-related effects on translation, which can occasionally be seen with the pFRYC controls.]]
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[[File:UT_Austin_2014_Kit_Incorporation_Value_Graph.png|600px|thumb|'''Figure 5.''' Incorporation values for each synthetase/tRNA pair.  The dashed line equals an incorporation value of 1.  Values greater than 1 when using pFRY indicate high efficiency and fidelity of ncAA incorporation.  The GFP:RFP relative fluorescence values in the presence and absence of ncAA (see '''Figure 4''') were used to calculate incorporation values.  Values were determined by dividing the GFP:RFP relative fluorescence in the presence of ncAA by the GFP:RFP relative fluorescence in the absence of ncAA. Data are presented as the average of three independent cultures. Error bars denote standard deviation.]]
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The incorporation value is a single number that measure the relative efficiency and fidelity of a ncAA tRNA synthetase/tRNA pair.  A value of 1 or lower indicates no significant incorporation dependent on the presence of ncAA in the culture.  The higher the value, the higher the fidelity and/or efficiency of the synthetase/tRNA pair.  It is important to note that ncAA-related effects on growth and translation can reduce the incorporation value of a synthetase/tRNA pair.  At this time, we believe this is the most telling form of an incorporation value.
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The synthetase/tRNA pairs that showed the highest incorporation values include AzF, 3-nitrotyrosine, ONBY, and 3-iodotyrosine in decreasing order. Among the ncAAs tested, ONBY consistently slowed the growth rate of the culture significantly (as seen by OD600 readings, data not shown) suggesting possible toxicity to the cell.  However, ncAA incorporation remained relatively high, resulting in a good incorporation value.  Synthetase/tRNA pairs that showed the lowest levels of ncAA incorporation include 3-aminotyrosine, <small>L</small>-DOPA, and CNF.
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We wanted a way to better summarize the output of the kit with a single measurement value. We decided to calculate an overall '''incorporation value''' as the GFP:RFP relative fluorescence value in the presence of the ncAA divided by the GFP:RFP relative fluorescence value when the ncAA is not included in the culture. Thus, the incorporation value is a single number that measures the relative efficiency and fidelity of a ncAA tRNA synthetase/tRNA pair.  A value of 1 indicates no significant dependence of incorporation on the presence of ncAA in the culture.  The higher the value, the higher the fidelity and/or efficiency of the synthetase/tRNA pair.  It is important to note that ncAA-related effects on growth and translation can also reduce the apparent incorporation value of a synthetase/tRNA pair below 1.
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'''The synthetase/tRNA pairs that showed the highest incorporation values were AzF, 3-nitrotyrosine, ONBY, and 3-iodotyrosine.''' Among the ncAAs tested, ONBY consistently slowed the growth rate of the culture significantly (as seen by OD<sub>600</sub> readings) suggesting possible toxicity to the cell.  However, ncAA incorporation remained relatively high, resulting in a good incorporation value.  '''Synthetase/tRNA pairs that showed the lowest levels of ncAA incorporation included 3-amino-<small>L</small>-tyrosine, <small>L</small>-DOPA, and CNF.'''
<h1>Discussion</h1>
<h1>Discussion</h1>
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Our ncAA measurement kit was able to successfully compare the fidelity and efficiency of seven different synthetase/tRNA pairs. We were able to confidently say that one synthetase/tRNA pair had a higher fidelity than another.  We saw clear evidence that three of our tRNA synthetase/tRNA pairs seemed incapable of discriminating between their ncAA and the 20 canonical amino acids present in media: 3-aminotyrosine, <small>L</small>-DOPA, and CNF.  We were able to test triplicate cultures of seven different ncAAs and tyrosine (eight total synthetase/tRNA pairs) in one day, generating results that immediately told us which ncAAs worked best in our system both in terms of fidelity and efficiency of incorporation.  This required no advanced training or access to equipment besides a shaker and a fluorometer.
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Our ncAA measurement kit was able to successfully compare the fidelity and efficiency of seven different synthetase/tRNA pairs. We were able to confidently say that one synthetase/tRNA pair had a higher fidelity than another.  '''We saw clear evidence that three of our tRNA synthetase/tRNA pairs seemed incapable of discriminating between their ncAA and the 20 canonical amino acids present in media: 3-amino-<small>L</small>-tyrosine, <small>L</small>-DOPA, and CNF.''' We were able to test triplicate cultures of seven different ncAAs and tyrosine (eight total synthetase/tRNA pairs) in one day, generating results that immediately told us which ncAAs worked best in our system both in terms of fidelity and efficiency of incorporation.  This required no advanced training or access to equipment besides a shaker and a fluorometer.
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While the measurements may not be perfectly accurate due to the nature of this test, the measurement kit is designed more around ease of use, cost-efficiency, and portability. The ncAA measurement kit can be used to quickly test a synthetase/tRNA pair's quality with minimal effort, as opposed to other more accurate but more intensive or expensive measures such as mass spectrometry. While mass spectrometry can give much more definitive information about a synthetase/tRNA pair, there are many different factors that could make it unreasonable for undergraduate research. It is a technique that requires a fair amount of skill to do properly, and can be very costly as well.  Additionally, the sample needs to be purified from cell culture and prepped for mass spectrometry.
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While the measurements may not be perfectly accurate due to the nature of this test, the measurement kit is designed more around ease of use, cost-efficiency, and portability. The ncAA measurement kit can be used to quickly test a synthetase/tRNA pair's quality with minimal effort, as opposed to other more accurate but more intensive or expensive measures such as mass spectrometry. While mass spectrometry can give much more definitive information about a synthetase/tRNA pair, there are many different factors that could make it unreasonable for undergraduate research or high-throughput use. It is a technique that requires a fair amount of skill to do properly, and can be very costly as well.  Additionally, the sample needs to be purified from cell culture and prepped for mass spectrometry.
For the ncAA measurement kit, all that is necessary is to request from us the kit plasmids (pFRYC and PFRY in separate strains of amberless ''E. coli''), which we are immediately making available to anyone who requests the Expanded Genetic Code Measurement Kit.  Once you receive the frozen cultures (or plasmids), transform the synthetase/tRNA pair that you wish to test into the two different cell strains, and run the experiment. Thus, if you receive the measurement kit on Monday, you could have your synthetase/tRNA pairs characterized by Friday.  The kit can also be used to test how one or more synthetase/tRNA pairs work in different cells or under different conditions.  However, in this case, you may need to retransform the kit plasmids into the different strain.
For the ncAA measurement kit, all that is necessary is to request from us the kit plasmids (pFRYC and PFRY in separate strains of amberless ''E. coli''), which we are immediately making available to anyone who requests the Expanded Genetic Code Measurement Kit.  Once you receive the frozen cultures (or plasmids), transform the synthetase/tRNA pair that you wish to test into the two different cell strains, and run the experiment. Thus, if you receive the measurement kit on Monday, you could have your synthetase/tRNA pairs characterized by Friday.  The kit can also be used to test how one or more synthetase/tRNA pairs work in different cells or under different conditions.  However, in this case, you may need to retransform the kit plasmids into the different strain.
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We are optimistic that this measurement kit can help speed up the process of developing a new synthetase/tRNA pair, as well as characterizing large groups of synthetase/tRNA pairs, as we now have a way to quickly, cheaply, and easily do large scale characterizations.
 
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Due to the nature of the Expanded Genetic Code Measurement Kit, <i>in vivo</i> influences will affect certain data and results. This knowledge is very useful by providing a broader and biological perspective of <i>in vivo</i> perspective of cellular health. In general, the presence of ncAAs slowed the growth of amberless ''E. coli'', sometimes quite significantly. This knowledge, as seen through the GFP:RFP ratio, can be very informative when assessing whether to use a ncAA tRNA synthetase/tRNA pair.
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We are optimistic that this measurement kit can help speed up the process of developing a new synthetase/tRNA pairs, as well as characterizing large groups of synthetase/tRNA pairs, as we now have a way to quickly, cheaply, and easily do large scale characterizations. For example, we could now systematically test how changing the expression levels of a synthetase and its tRNA alters the efficiency and fidelity of ncAA incorporation.
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Due to the nature of the Expanded Genetic Code Measurement Kit, <i>in vivo</i> influences will affect certain data and results. This knowledge is very useful by providing a broader and biological perspective of cellular health. In general, the presence of ncAAs slowed the growth of amberless ''E. coli'', sometimes quite significantly. This knowledge, as seen through the GFP:RFP ratio, can be very informative when assessing whether to use a ncAA tRNA synthetase/tRNA pair.
<h1>Conclusion</h1>
<h1>Conclusion</h1>
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This year the UT Austin iGEM Team has chosen to take part in the [https://2014.igem.org/Tracks/Measurement Measurement Track] of the iGEM competition.  We have presented here the Expanded Genetic Code Measurement Kit for the purpose of quickly characterizing novel ncAA tRNA synthetase/tRNA pairs, which meet the [https://2014.igem.org/Team:Austin_Texas/medal_requirements medal criteria].  Prior to this measurement kit there was not a widely available and easily accessible kit for assessing ncAA tRNA synthetase/tRNA pairs.  Although numerous labs have used mass spectrometry, such a technique is not always cheap not widely available.  Additionally, we have begun the process of standardization for ncAA synthetase/tRNA pairs by using our kit to simultaneously characterize seven different ncAA synthetase/tRNA pairs as well as a tyrosine RS. '''This method of testing was designed to be easy-to-use, portable, quicker, and more available than other methods of characterization and analysis.  We are optimistic that this is a first step in opening the doorway to the usage of ncAAs for more iGEM labs and research.'''
+
This year the UT Austin iGEM Team has chosen to take part in the [https://2014.igem.org/Tracks/Measurement Measurement Track] of the iGEM competition.  We have presented here the Expanded Genetic Code Measurement Kit for the purpose of quickly characterizing novel ncAA tRNA synthetase/tRNA pairs, which meet the [https://2014.igem.org/Team:Austin_Texas/medal_requirements medal criteria].  Prior to this measurement kit there was not a widely available and easily accessible kit for assessing ncAA tRNA synthetase/tRNA pairs.  Although numerous labs have used mass spectrometry, such a technique is not always cheap not widely available.  Additionally, we have begun the process of standardization for ncAA synthetase/tRNA pairs by using our kit to simultaneously characterize seven different ncAA synthetase/tRNA pairs as well as a tyrosine RS. '''This method of testing was designed to be easy-to-use, portable, quicker, and more available than other methods of characterization and analysis.  We are optimistic that this is a first step in opening the doorway to more iGEM teams and labs using these new chemical building blocks in their projects.'''
Documentation, including sequence information, of the tRNA synthetase/tRNA pairs used can be found [https://2014.igem.org/Team:Austin_Texas/kit#ncAA_Synthetase_Table below].
Documentation, including sequence information, of the tRNA synthetase/tRNA pairs used can be found [https://2014.igem.org/Team:Austin_Texas/kit#ncAA_Synthetase_Table below].
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| 307.09
| 307.09
| Soluble in water<br> Heat to 70°C and vortex to dissolve  
| Soluble in water<br> Heat to 70°C and vortex to dissolve  
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| Stock Concentration: 10mM <br>(.122g in 10mL H20)<br> Concentration in Culture: 1mM
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| Stock Concentration: 10mM <br>(.03g in 10mL H2O)<br> Concentration in Culture: 1mM
|-
|-

Latest revision as of 23:54, 18 March 2015