Difference between revisions of "Part:BBa K1189027"
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<partinfo>BBa_K1189027 short</partinfo>
 
<partinfo>BBa_K1189027 short</partinfo>
  
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E/K coils are synthetic coiled-coil domains designed specifically to bind to each other with high affinity and specificity (Litowski and Hodges, 2002). They are composed of a heptad repeat that forms a coil structures that are able to interact with each other. These coils are able to interact with each other in an anti-parallel fashion that makes them useful for applications such as peptide capture, protein purification and in biosensors. For our project we decided to make use of the IAAL E3/K3 coils (BBa_K118901, BBa_K1189011) due to the balance they offer between affinity and specificity. These parts were already in the registry, however the DNA was never received, so we built, sequenced and re-submitted them.
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<html>
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E/K coils are synthetic coiled-coil domains designed specifically to bind to each other with high affinity and specificity (Litowski and Hodges, 2002) (Figure 1). They are composed of a heptad repeat that forms a coil structures that are able to interact with each other. These coils are able to interact with each other in an anti-parallel fashion that makes them useful for applications such as peptide capture, protein purification and in biosensors. For our project we decided to make use of the IAAL E3/K3 coils (BBa_K118901, BBa_K1189011) due to the balance they offer between affinity and specificity (Table 1).
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<figure>
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<img src="https://static.igem.org/mediawiki/2013/a/a9/UCalgary2013TRCoilrenderpng.png" alt="Coiled-coils" width="193" height="300">
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<figcaption>
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<p><b>Figure 1.</b> Ribbon visualization of the E3/K3 IAAL coiled-coils.</p>
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</figcaption>
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</figure>
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<center><b>Table 1. Coil Peptide Sequences</b></center>
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<center><table width="400" border="1">
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  <tr>
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    <td>Coil Name</td>
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    <td>Peptide Sequence</td>
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  </tr>
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  <tr>
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    <td>IAAL E3</td>
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    <td>NH<sub>2</sub>-EIAALEKEIAALEKEIAALEK-COOH</td>
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  </tr>
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  <tr>
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    <td>IAAL K3</td>
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    <td>NH<sub>2</sub>-KIAALKEKIAALKEKIAALKE-COOH</td>
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  </tr>
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</table></center>
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<p>These E3/K3 coils are able to form heterodimers due to the hydrophobic residues contained within the heptad repeat. In our case these are isoleucine and leucine residues. Designated by empty arrows in the helical wheel diagram below (Figure 2) these residues form the core of the binding domain of the coils. In order to prevent the homodimerization of these coils charged residues are included in the design. The electrostatic interactions between glutamic acid and lysine residues prevent an E-coil from binding with an E-coil for example. These parts were already in the registry, however the DNA was never received, so we built, sequenced and re-submitted them.</p>
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<figure>
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<img src="https://static.igem.org/mediawiki/2013/3/37/UCalgary2013TRCoildiagramtransparent2.png" alt="IAAL E3/K3 Coil Helical Wheel Diagram" width="800" height="448">
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<figcaption>
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<p><b>Figure 2.</b> A helical wheel representation of the IAAL E3/K3 coiled-coil heterodimer viewed as a cross-section based off of a similar figure created by Litowski and Hodges (2002). The peptide chain propagates into the page from the N- to the C- terminus. Hydrophobic interactions between the coils are indicated by the clear wide arrows. The intermolecular electrostatic interactions between the coils are displayed by the thin curved arrow (eg. Between Glu<sup>15</sup> and Lys<sup>20</sup>) Letters a, b, c,and d designate the positions of IAAL repeat in the heptapeptide. The e and g positions are occupied by the charged residues.</p>
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</figcaption>
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</figure> </html>
  
 
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<span class='h3bb'>Sequence and Features</span>
 
<span class='h3bb'>Sequence and Features</span>
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<partinfo>BBa_K1189027 SequenceAndFeatures</partinfo>
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<partinfo>BBa_K1189015 SequenceAndFeatures</partinfo>
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Revision as of 07:41, 28 September 2013

K coil

E/K coils are synthetic coiled-coil domains designed specifically to bind to each other with high affinity and specificity (Litowski and Hodges, 2002) (Figure 1). They are composed of a heptad repeat that forms a coil structures that are able to interact with each other. These coils are able to interact with each other in an anti-parallel fashion that makes them useful for applications such as peptide capture, protein purification and in biosensors. For our project we decided to make use of the IAAL E3/K3 coils (BBa_K118901, BBa_K1189011) due to the balance they offer between affinity and specificity (Table 1).

Coiled-coils

Figure 1. Ribbon visualization of the E3/K3 IAAL coiled-coils.

Table 1. Coil Peptide Sequences
Coil Name Peptide Sequence
IAAL E3 NH2-EIAALEKEIAALEKEIAALEK-COOH
IAAL K3 NH2-KIAALKEKIAALKEKIAALKE-COOH

These E3/K3 coils are able to form heterodimers due to the hydrophobic residues contained within the heptad repeat. In our case these are isoleucine and leucine residues. Designated by empty arrows in the helical wheel diagram below (Figure 2) these residues form the core of the binding domain of the coils. In order to prevent the homodimerization of these coils charged residues are included in the design. The electrostatic interactions between glutamic acid and lysine residues prevent an E-coil from binding with an E-coil for example. These parts were already in the registry, however the DNA was never received, so we built, sequenced and re-submitted them.

IAAL E3/K3 Coil Helical Wheel Diagram

Figure 2. A helical wheel representation of the IAAL E3/K3 coiled-coil heterodimer viewed as a cross-section based off of a similar figure created by Litowski and Hodges (2002). The peptide chain propagates into the page from the N- to the C- terminus. Hydrophobic interactions between the coils are indicated by the clear wide arrows. The intermolecular electrostatic interactions between the coils are displayed by the thin curved arrow (eg. Between Glu15 and Lys20) Letters a, b, c,and d designate the positions of IAAL repeat in the heptapeptide. The e and g positions are occupied by the charged residues.

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal NgoMIV site found at 230
  • 1000
    COMPATIBLE WITH RFC[1000]