Evaluation of residue variability in a conformation-specific context and during evolutionary sequence reconstruction narrows drug resistance selection in Abl1 tyrosine kinase

Autor(es)

Otsuka, Felipe A. M. ; Bjelic, Sinisa

• Tipo de documento: Artigo Científico
• Fonte: Protein Science; v. 31, n. 7, p. 14-pg., 2022-07-01.

Resumo

Diseases with readily available therapies may eventually prevail against the specific treatment by the acquisition of resistance. The constitutively active Abl1 tyrosine kinase known to cause chronic myeloid leukemia is an example, where patients may experience relapse after small inhibitor drug treatment. Mutations in the Abl1 tyrosine kinase domain (Abl1-KD) are a critical source of resistance and their emergence depends on the conformational states that have been observed experimentally: the inactive state, the active state, and the intermediate inactive state that resembles Src kinase. Understanding how resistant positions and amino acid identities are determined by selection pressure during drug treatment is necessary to improve future drug development or treatment decisions. We carry out in silico site-saturation mutagenesis over the Abl1-KD structure in a conformational context to evaluate the in situ and conformational stability energy upon mutation. Out of the 11 studied resistant positions, we determined that 7 of the resistant mutations favored the active conformation of Abl1-KD with respect to the inactive state. When, instead, the sequence optimization was modeled simultaneously at resistant positions, we recovered five known resistant mutations in the active conformation. These results suggested that the Abl1 resistance mechanism targeted substitutions that favored the active conformation. Further sequence variability, explored by ancestral reconstruction in Abl1-KD, showed that neutral genetic drift, with respect to amino acid variability, was specifically diminished in the resistant positions. Since resistant mutations are susceptible to chance with a certain probability of fixation, combining methodologies outlined here may narrow and limit the available sequence space for resistance to emerge, resulting in more robust therapeutic treatments over time. (AU)

• Processo FAPESP: 19/25955-0 - Reconstrução de sequências enzimáticas ancestrais para entender o câncer: capacidade de evolução e resistência da tirosina quinase Abl1
• Beneficiário: Felipe Akihiro Melo Otsuka
• Modalidade de apoio: Bolsas no Exterior - Estágio de Pesquisa - Doutorado Direto
• Processo FAPESP: 18/18537-4 - Relação da estrutura quaternária e atividade enzimática da beta-glicosidase de Spodoptera frugiperda (Sfbgly)
• Beneficiário: Felipe Akihiro Melo Otsuka
• Modalidade de apoio: Bolsas no Brasil - Doutorado Direto