Difference between revisions of "Part:BBa K404223"
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<partinfo>BBa_K404223 short</partinfo> | <partinfo>BBa_K404223 short</partinfo> | ||
− | <br><b>The RGD integrin binding motif, inserted into https://parts.igem.org/wiki/index.php?title=Part: | + | <br><b>The RGD integrin binding motif, inserted into <a class="noul_link" href="https://parts.igem.org/wiki/index.php?title=Part:BBa_K404003">BBa_K404003</a></b> |
[[Image:Freiburg10_Rep-VP123_P5-TATA-less 453-RGD.png|thumb|center|480px]]<br> | [[Image:Freiburg10_Rep-VP123_P5-TATA-less 453-RGD.png|thumb|center|480px]]<br> |
Revision as of 22:04, 25 October 2010
[AAV2]-Rep-VP123_p5-TATAless (ViralBrick-453-RGD)
The RGD integrin binding motif, inserted into <a class="noul_link" href="https://parts.igem.org/wiki/index.php?title=Part:BBa_K404003">BBa_K404003</a>
Usage and Biology
Integrins are transmembrane proteins that, among other functions, mediate cell attachment to surrounding tissues. They bind to a motif consisting of the amino acids arginine, glycine and aspartic acid (RGD in one-letter code). Because Integrin is highly expressed in many tumor cell lines (Albelda et al., 1990), (Damjanovich, Albelda, Mette, & Buck, 1992), (Lessey et al., 1995), (Smythe, LeBel, Bavaria, Kaiser, & Albelda, 1995), (Gladson & Cheresh, 1991), AAV particles displaying the RGD motif on various positions in their capsid proteins have been created by (Shi et al., 2003). Particles displaying RGD at amino acid positions 584 & 588 as well as 453 or 587 (Boucas et al., 2009) showed transduction efficiencies similar to wt AAV, even when the cells’ HSPG receptors were blocked by heparin sulfate or when the natural HSPG binding motif on the capsid surface was knocked out. To further broaden the area of therapeutic application, we created a ViralBrick containing the RGD motive to specifically target cells with low HSPG-/high Integrin expression.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BamHI site found at 3644
Illegal XhoI site found at 1913
Illegal XhoI site found at 2099 - 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 4170
Illegal BsaI site found at 4352
Illegal BsaI site found at 4389
Illegal SapI site found at 3048