Study of the structural pathology caused by CYP2C9 polymorphisms towards flurbiprofen metabolism using molecular dynamics simulation

Conference proceedings article

ผู้เขียน/บรรณาธิการ

กลุ่มสาขาการวิจัยเชิงกลยุทธ์

ไม่พบข้อมูลที่เกี่ยวข้อง

รายละเอียดสำหรับงานพิมพ์

รายชื่อผู้แต่ง: Saikatikorn Y., Lertkiatmongkol P., Assawamakin A., Ruengjitchatchawalya M., Tongsima S.

ผู้เผยแพร่: Springer Verlag (Germany): Computer Proceedings

ปีที่เผยแพร่ (ค.ศ.): 2010

Volume number: 115 CCIS

หน้าแรก: 26

หน้าสุดท้าย: 35

จำนวนหน้า: 10

ISBN: 3642167497; 9783642167492

นอก: 1865-0929

URL: https://www.scopus.com/inward/record.uri?eid=2-s2.0-78649573472&doi=10.1007%2f978-3-642-16750-8_3&partnerID=40&md5=8c4bf6e34f508586d65acc955a9ca29d

ภาษา: English-Great Britain (EN-GB)

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บทคัดย่อ

CYP2C9 is one of the major cytochrome P450 enzymes that play a crucial role in metabolic clearance of several drugs in the current clinical used. CYP2C9 has several allelic variant forms each of which arises from single amino acid substitution and could reduce/increase enzyme activities and affect drug metabolism. Mutant alleles may cause serious toxicity in some narrow therapeutic index drugs. CYP2C9*13, one of the CYP2C9 variant forms that is commonly found in Asian population, has a Leu90Pro amino acid substitution that leads to defective drug metabolism in individuals who carry this allele. It has been reported that metabolic activity of CYP2C9*13 was reduced towards some CYP2C9 substrates compared to wildtype. In this study, X-ray crystal structure of human cytochrome P450 2C9 complexed with flurbiprofen (PDB code: 1R9O) was represented to wildtype and the structure of CYP2C9*13 was constructed based on the X-ray crystal structure of CYP2C9-flurbiprofen complex. Herein, molecular docking of CYP2C9*1 and CYP2C9*13 with flurbiprofen was performed in search for flurbiprofen orientation that corresponds to its binding state before undergoing monooxygenation. Subsequently, molecular dynamics simulation was operated to compare binding of flurbiprofen in catalytic cavity of these 2 variants. Substrate access channel of CYP2C9*13 has a dramatic effect on an interaction between the drug and the enzyme. Consequently, this study can lead to an understanding of structural pathology caused by single amino acid change in CYP2C9*13 variant. ฉ 2010 Springer-Verlag Berlin Heidelberg.

คำสำคัญ

CYP2C9*13, Cytochrome P450 2C9, Flurbiprofen, Genetic polymorphisms