Development of split luciferase complementation probes sensing KRAS/effector interaction
Author:
Affiliation:
1. CarnaBio USA, Inc., 400 Oyster Point Boulevard, Suite 525, South San Francisco, CA 94080, U.S.A.
2. Carna Biosciences, Inc., 1-5-5 Minatojima-Minamimachi, BMA 3rd Floor, Chuo-ku, Kobe, Hyogo 650-0047, Japan
Publisher
AMED iD3 Catalyst Unit
Link
https://www.jstage.jst.go.jp/article/trs/1/2/1_1909/_pdf
Reference37 articles.
1. 1. Papke, B. and Der, C. J. 2017. Drugging RAS: Know the enemy. Science 355: 1158–1163.
2. 2. Keeton, A. B., Salter, E. A. and Piazza, G. A. 2017. The RAS-effector interaction as a drug target. Cancer Res. 77: 221–226.
3. 3. Barnard, D., Sun, H., Baker, L. and Marshall, M. S. 1998. In vitro inhibition of Ras-Raf association by short peptides. Biochem. Biophys. Res. Commun. 247: 176–180.
4. 4. Gus-Brautbar, Y., Johnson, D., Zhang, L., Sun, H., Wang, P., Zhang, S., Zhang, L. and Chen, Y. H. 2012. The anti-inflammatory TIPE2 is an inhibitor of the oncogenic Ras. Mol. Cell 45: 610–618.
5. 5. McGee, J. H., Shim, S. Y., Lee, S. J., Swanson, P. K., Jiang, S. Y., Durney, M. A. and Verdine, G. L. 2018. Exceptionally high-affinity Ras binders that remodel its effector domain. J. Biol. Chem. 293: 3265–3280.
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