Experimental variables determine the outcome of RAS-RAS interactions

Zhiwei Zhou, Tra Ly Nguyen, Xingxiao Li, Christel Poujol, Ewa Berlinska, Sandra Vietti Michelina, Jonas N. Kapp, Andreas Plückthun, Monte M. Winslow, Chiara Ambrogio, Yibing Shan, David Santamaría, Kenneth D. Westover

Research output: Contribution to journalArticlepeer-review

Abstract

RAS clustering at the cell membrane is critical to activate signaling in cells, but whether this clustering is mediated exclusively by its c-terminal hypervariable region, receives contributions from the G-domain of RAS, and/or is influenced by secondary effectors has been intensely debated. Reports that G-domain mutations do not modulate RAS-RAS interactions have led some to question the validity of previous experiments that indicate the G-domain plays a role in RAS clustering/interactions. Here we reconcile these findings by clarifying the impact of experimental variables, such as protein expression levels, cellular context, RAS zygosity, and secondary effector interactions on RAS clustering. Lack of control over these variables impacts the results using G-domain mutations across various assay systems and can lead to unsound conclusions.

Original languageEnglish (US)
Article number107859
JournalJournal of Biological Chemistry
Volume300
Issue number11
DOIs
StatePublished - Nov 2024

Keywords

  • D154Q
  • G-domain
  • KRAS
  • RAS clustering
  • membrane complex

ASJC Scopus subject areas

  • Biochemistry
  • Molecular Biology
  • Cell Biology

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