Nature Communications (Jun 2021)
RAS-inhibiting biologics identify and probe druggable pockets including an SII-α3 allosteric site
- Katarzyna Z. Haza,
- Heather L. Martin,
- Ajinkya Rao,
- Amy L. Turner,
- Sophie E. Saunders,
- Britta Petersen,
- Christian Tiede,
- Kevin Tipping,
- Anna A. Tang,
- Modupe Ajayi,
- Thomas Taylor,
- Maia Harvey,
- Keri M. Fishwick,
- Thomas L. Adams,
- Thembaninkosi G. Gaule,
- Chi H. Trinh,
- Matthew Johnson,
- Alexander L. Breeze,
- Thomas A. Edwards,
- Michael J. McPherson,
- Darren C. Tomlinson
Affiliations
- Katarzyna Z. Haza
- School of Molecular and Cellular Biology, Astbury Centre for Structural and Molecular Biology, University of Leeds
- Heather L. Martin
- School of Molecular and Cellular Biology, Astbury Centre for Structural and Molecular Biology, University of Leeds
- Ajinkya Rao
- School of Molecular and Cellular Biology, Astbury Centre for Structural and Molecular Biology, University of Leeds
- Amy L. Turner
- School of Molecular and Cellular Biology, Astbury Centre for Structural and Molecular Biology, University of Leeds
- Sophie E. Saunders
- School of Molecular and Cellular Biology, Astbury Centre for Structural and Molecular Biology, University of Leeds
- Britta Petersen
- School of Molecular and Cellular Biology, Astbury Centre for Structural and Molecular Biology, University of Leeds
- Christian Tiede
- School of Molecular and Cellular Biology, Astbury Centre for Structural and Molecular Biology, University of Leeds
- Kevin Tipping
- School of Molecular and Cellular Biology, Astbury Centre for Structural and Molecular Biology, University of Leeds
- Anna A. Tang
- School of Molecular and Cellular Biology, Astbury Centre for Structural and Molecular Biology, University of Leeds
- Modupe Ajayi
- School of Molecular and Cellular Biology, Astbury Centre for Structural and Molecular Biology, University of Leeds
- Thomas Taylor
- School of Molecular and Cellular Biology, Astbury Centre for Structural and Molecular Biology, University of Leeds
- Maia Harvey
- School of Molecular and Cellular Biology, Astbury Centre for Structural and Molecular Biology, University of Leeds
- Keri M. Fishwick
- School of Molecular and Cellular Biology, Astbury Centre for Structural and Molecular Biology, University of Leeds
- Thomas L. Adams
- School of Molecular and Cellular Biology, Astbury Centre for Structural and Molecular Biology, University of Leeds
- Thembaninkosi G. Gaule
- School of Molecular and Cellular Biology, Astbury Centre for Structural and Molecular Biology, University of Leeds
- Chi H. Trinh
- School of Molecular and Cellular Biology, Astbury Centre for Structural and Molecular Biology, University of Leeds
- Matthew Johnson
- Avacta Life Sciences
- Alexander L. Breeze
- School of Molecular and Cellular Biology, Astbury Centre for Structural and Molecular Biology, University of Leeds
- Thomas A. Edwards
- School of Molecular and Cellular Biology, Astbury Centre for Structural and Molecular Biology, University of Leeds
- Michael J. McPherson
- School of Molecular and Cellular Biology, Astbury Centre for Structural and Molecular Biology, University of Leeds
- Darren C. Tomlinson
- School of Molecular and Cellular Biology, Astbury Centre for Structural and Molecular Biology, University of Leeds
- DOI
- https://doi.org/10.1038/s41467-021-24316-0
- Journal volume & issue
-
Vol. 12,
no. 1
pp. 1 – 15
Abstract
Oncogenic RAS mutants remain difficult to target with small molecules. Here, the authors show that RAS-binding Affimer proteins inhibit RAS signaling while binding diverse regions on the RAS surface, suggesting the potential to use Affimers as tools to identify new binding pockets and pharmacophores.