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Poster display session

104P - Development New Generation of Imatinib Using Structural Biology Techniques at Ambient Temperature

Date

15 Oct 2022

Session

Poster display session

Presenters

Gözde Usta

Citation

Annals of Oncology (2022) 33 (suppl_8): S1383-S1430. 10.1016/annonc/annonc1095

Authors

G. Usta

Author affiliations

  • Koc University Hospital, Istanbul/TR

Resources

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Abstract 104P

Background

Chronic myeloid leukemia (CML) is a kind of blood cancer and most CML patients have associated with a chromosomal anomaly with the BCR-ABL fusion oncogene, which occurs as a result of translocation between the Abelson murine leukemia (ABL1) gene on chromosome 9 and breakpoint cluster region (BCR) gene on chromosome 22. Imatinib mesylate is the first small molecule developed to target the BCR-ABL fusion protein. Imatinib reduces BCR-ABL activity by binding to the inactive conformation of tyrosine kinases. Despite a high response rate in CML patients with imatinib therapy, almost one-third of patients still have an inadequate response to Imatinib. In other words, mutations in the imatinib-binding pocket or other regions of the BCR-ABL kinase result in various resistances to imatinib in CML patients. Therefore, there have revealed a need to develop a more potent new molecule with an imatinib function that is more resistant to mutations.

Methods

In this study, ABL kinase domain gene was purchased from Genscript Biotech. The gene was inserted to pET11a vector plasmid construct. The plasmid was transformed into E.coli, strain BL21 (Rosetta-2). Transformed E. coli were grown overnight on agar plates. The colonies were collected from agar plates and started large volume of culture in rich LB media. To be able to procure further purified protein, we were used Ni-NTA affinity chromatography. The purified protein solution was added to crystal screen conditions in Terasaki plates. Then, X-ray diffraction images were collected from the formed crystals in order to acquire the best 3D structure. These diffraction datas were collected from XtalCheck module (Rigaku Oxford Diffraction) at ambient temperature.

Results

We will have revealed the structures determined at ambient temperature and high resolution with the help of X-ray crystallography technique. Additionally, we will have re-evaluated structures and designed new target small molecule with approaching from the perspective of integrative structural biology.

Conclusions

The results propose that may developed a new generation of Imatinib that is more specific, high affinity and resistant to possible mutations to treat CML disease and improve patients’ lives.

Editorial acknowledgement

Hasan DeMirci, Department of Molecular Biology and Genetics, Koc University, Istanbul, Turkey; Koc University Isbank Center for Infectious Diseases (KUISCID), Istanbul, Turkey; Stanford PULSE Institute, SLAC National Laboratory, Menlo Park, CA, USA.

Legal entity responsible for the study

Koc University Structural Biology & Innovative Drug Development Center.

Funding

Koc University Structural Biology & Innovative Drug Development Center/ Deva pharmaceuticals Companies.

Disclosure

The author has declared no conflicts of interest.

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