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Chemotherapy Drug Response to the L858R-induced Conformational Change of EGFR Activation Loop in Lung Cancer

Chemotherapy Drug Response to the L858R-induced Conformational Change of EGFR Activation Loop in Lung Cancer

Xi Ding, Xingcai Liu, Xiaoyun Song, Jun Yao

Mol Inform. 2016 Oct;35(10):529-537.

PMID: 27643705

Abstract:

Oncogenic L858R mutation of human epidermal growth factor receptor (EGFR) confers constitutive activation to the kinase and is frequently observed in the pathological process of metastatic lung cancer. Selective inhibition of EGFRL858R mutant over wild-type EGFR (EGFRWT ) has been established as an attractive target for cancer chemotherapy. Here, we performed long-term molecular dynamics (MD) simulations to reconstruct the complete dynamics trajectory of L858R-induced conformational change in EGFR activation loop (A-loop). It was found that the mutation considerably destabilizes A-loop in Src-like inactive conformation and promotes the loop conversion to DFG-in active form. Electrostatic force is primarily responsible for the conversion and stabilization upon the mutation. Binding free energy analysis revealed that Gefitinib exhibits strong selectivity for mutant over wild-type kinases. The A-loop conformation, but not L858R mutation, directly determines inhibitor affinity; the mutation can indirectly influence inhibitor binding via regulation of A-loop conformation. Subsequently, chemical similarity searching was carried out with the structural sketch of Gefitinib against a large library of drug/lead-like compounds, from which two hits were identified to have high selectivity for EGFRL858R over EGFRW ; they can potently inhibit the kinase mutant with IC50 values at nanomolar level. The selectivity is primarily originated from hydrogen bond interactions of inhibitor ligands with mutant but not with wild type due to the A-loop conformational difference.

Chemicals Related in the Paper:

Catalog Number	Product Name	Structure	CAS Number	Price
IAR42413242	EGFR (L858R) Active human			Price

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