BRAF^Δβ3-αC in-frame deletion mutants differ in their dimerization propensity, HSP90 dependence, and druggability.

ABSTRACT: In-frame BRAF exon 12 deletions are increasingly identified in various tumor types. The resultant BRAF^Δβ3-αC oncoproteins usually lack five amino acids in the β3-αC helix linker and sometimes contain de novo insertions. The dimerization status of BRAF^Δβ3-αC oncoproteins, their precise pathomechanism, and their direct druggability by RAF inhibitors (RAFi) has been under debate. Here, we functionally characterize BRAF^ΔLNVTAP>F and two novel mutants, BRAF^delinsFS and BRAF^ΔLNVT>F, and compare them with other BRAF^Δβ3-αC oncoproteins. We show that BRAF^Δβ3-αC oncoproteins not only form stable homodimers and large multiprotein complexes but also require dimerization. Nevertheless, details matter as aromatic amino a

SUBMITTER: Lauinger M 

PROVIDER: S-EPMC11804575 | biostudies-literature | 2023 Sep

REPOSITORIES: biostudies-literature