Volume 112, Issue 6 e24165
REVIEW

Therapeutic peptides targeting the Ras superfamily

Catherine A. Hurd

Catherine A. Hurd

Department of Biochemistry, University of Cambridge, Cambridge, UK

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Helen R. Mott

Helen R. Mott

Department of Biochemistry, University of Cambridge, Cambridge, UK

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Darerca Owen

Corresponding Author

Darerca Owen

Department of Biochemistry, University of Cambridge, Cambridge, UK

Correspondence

Darerca Owen, Department of Biochemistry, University of Cambridge, 80 Tennis Court Road, Cambridge, UK.

Email: [email protected]

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First published: 13 April 2020
Citations: 9

Funding information: AstraZeneca; Biotechnology and Biological Sciences Research Council, Grant/Award Number: BB/M011194/1; Cambridge Cancer Centre; Glover Research Fund; Medical Research Council, Grant/Award Number: MR/K017101/1

Abstract

The Ras superfamily of small GTPases are master regulators of numerous essential processes within the cell, so that when they malfunction, cancer and many other diseases can result. For example, activating Ras mutations are present in approximately 20% of human cancers. As such, they are key therapeutic targets, yet more than three decades of intensive research efforts have failed to produce effective Ras inhibitors in the clinic. This is, in part, due to their relatively smooth surfaces which are difficult to target through traditional drug discovery methods using small molecules. Peptides offer a solution to this issue as they occupy larger surface areas on their targets and therefore offer exquisite selectivity and affinity. However, their use in the past has been limited to extracellular targets due to delivery issues. Recent advances in peptide macrocyclisation, modifications and delivery methods have ignited increased interest in the use of these highly effective biologics for intracellular targets. This review will cover progress made in the development of peptides targeting small GTPases to treat a wide range of diseases.

Graphical Abstract

CONFLICT OF INTEREST

The authors declare no competing interests.

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