DNA
HR2-Apt

Part:BBa_K3897000

Designed by: Connor   Group: iGEM21_GreatBay_SCIE   (2021-09-30)
Revision as of 01:44, 9 October 2021 by SoniaPeh (Talk | contribs)

HR2 Aptamer, for targeting HER2 receptors
HR2 Aptamer is an 86bp ssDNA strand that can be folded into 3D shapes to target Human Epidermal Growth Factor 2 (HER2)

Background

Human epidermal growth factor (HER2), belongs to the ErbB receptor tyrosine kinase family, involved in signal transduction pathways that regulate cell growth and differentiation. However, overexpression of HER2 can cause pathogenesis and progression of many carcinoma types. However, HER2 can also be used to treat these cancers. Current drugs like Herceptin bind HER2 through antibodies and inhibit its pathway, curing cancer. Some ADC drugs (Antibody-drug conjugates) also use HER2 as a target for binding, so drugs can be brought into proximity to the tumor cells. (e.g. T-DM1) Aptamers are oligonucleotides that form unique 3D structures that can bind to practically anything, ranging from small molecules like ions, amanitin; to large proteins like HER2 in our case. BBa_K3897000 is an aptamer, nicknamed HR2 aptamer, which specifically binds to HER2 ECD. HR2 aptamer is obtained from previous literature. It is synthesized through chemical synthesis, and its binding affinity for HER2 is tested through ELONA (An Enzyme-linked Oligonucleotide Assay).

T--GreatBay SCIE--HR2 Aptamer 2D.png
T--GreatBay SCIE--HR2 Aptamer 3D.png
Figure 1 2D(top) and 3D (bottom) simulations of HR2 aptamer, simulated by mFold and MATLAB, respecitively.

Experimental Data

We evaluated the HER2 binding affinity of the aptamer quantitatively. Methods were based on a type of sandwich ELISA Kit, HER2 proteins were incubated with increasing concentrations of FAM-labeled aptamer and analyzed by spectrofluorometer. Using non-linear regression analysis, the Kd of the aptamer for binding with the HER2 protein was estimated to be 1.803 μM. (See more in <a href="https://2021.igem.org/Team:GreatBay_SCIE/Results">Results</a>).

Figure 2 A further quantitative test for aptamer affinity. 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10 453 5Q451 4 449 3Q444 0 433 0Q418 0 415 7Q413 11 374 317L335 624L267 354Q200 88 200 79Q206 46 272 46H282Q288 41 289 37T286 19Q282 3 278 1Q274 0 267 0Q265 0 255 0T221 1T157 2Q127 2 95 1T58 0Q43 0 39 2T35 11Q35 13 38 25T43 40Q45 46 65 46Q135 46 154 86Q158 92 223 354T289 629Z"></path></defs><g stroke="currentColor" fill="currentColor" stroke-width="0" transform="matrix(1 0 0 -1 0 0)"><use xlink:href="#E2-MJMATHI-59" x="0" y="0"></use><use xlink:href="#E2-MJMAIN-3D" x="1040" y="0"></use><g transform="translate(1818,0)"><g transform="translate(397,0)"><rect stroke="none" width="3208" height="60" x="0" y="220"></rect><g transform="translate(60,393)"><use transform="scale(0.707)" xlink:href="#E2-MJMATHI-42" x="0" y="0"></use><use transform="scale(0.707)" xlink:href="#E2-MJMATHI-6D" x="759" y="0"></use><use transform="scale(0.707)" xlink:href="#E2-MJMATHI-61" x="1636" y="0"></use><use transform="scale(0.707)" xlink:href="#E2-MJMATHI-78" x="2165" y="0"></use><use transform="scale(0.707)" xlink:href="#E2-MJMAIN-D7" x="2737" y="0"></use><use transform="scale(0.707)" xlink:href="#E2-MJMATHI-58" x="3516" y="0"></use></g><g transform="translate(253,-410)"><use transform="scale(0.707)" xlink:href="#E2-MJMAIN-28" x="0" y="0"></use><use transform="scale(0.707)" xlink:href="#E2-MJMATHI-4B" x="389" y="0"></use><use transform="scale(0.707)" xlink:href="#E2-MJMATHI-64" x="1278" y="0"></use><use transform="scale(0.707)" xlink:href="#E2-MJMAIN-2B" x="1800" y="0"></use><use transform="scale(0.707)" xlink:href="#E2-MJMATHI-58" x="2579" y="0"></use><use transform="scale(0.707)" xlink:href="#E2-MJMAIN-29" x="3431" y="0"></use></g></g></g><use xlink:href="#E2-MJMAIN-2B" x="5767" y="0"></use><use xlink:href="#E2-MJMATHI-4D" x="6767" y="0"></use><use xlink:href="#E2-MJMAIN-D7" x="8040" y="0"></use><use xlink:href="#E2-MJMATHI-58" x="9041" y="0"></use></g></svg><script type="math/tex">Y=\frac{Bmax \times X}{(Kd +X)} + M \times X</script>. The R2 value for the curve is 0.9801 and Kd = 1.803 μM.

Sequence and Features

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
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]

Reference

  1. Liu, Z., Duan, J. H., Song, Y. M., Ma, J., Wang, F. D., Lu, X., & Yang, X. D. (2012). Novel HER2 aptamer selectively delivers cytotoxic drug to HER2-positive breast cancer cells in vitro. Journal of translational medicine, 10, 148.https://doi.org/10.1186/1479-5876-10-148


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Categories
Parameters
None