Varun Dewaker, Sung Taek Park, Jae Jun Lee* and Hyeong Su Kim*,
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The selected molecules were CID24326943, CID24459131, CID46375999, CID46533890, and CID55836895. MD simulations (200 ns) revealed stable CT83-ligand complexes, with MMPBSA calculations showing that Z839878730, CID24459131, and CID46375999 exhibited the most favorable relative binding free energies. Among these, CID46375999 shared greater similarity with the reference compound, featuring a 1,3,4-thiadiazole-2-carboxamide scaffold, hydrophobic properties, and hydrogen bonding potential. In contrast, CID24459131, which features an imidazolidinone ring and relatively bulky substituents such as a diphenylethyl moiety, exhibits a more flexible and extended conformation. Although CID46375999 contains a piperidine ring, its overall structure is more conformationally constrained compared to CID24459131, likely due to fewer rotatable bonds and a more compact architecture. Overall, CID46375999 aligned more closely with the reference compound in terms of chemical properties. Interaction fingerprint analysis revealed frequent interactions with key residues Leu15, Ile16, Phe18, Trp19, Arg22, Leu38, Arg42, Pro43, Arg76, Gln77, and Ile80, including hydrophobic interactions, π-stacking (Phe18 and Trp19), and H-bonds (Arg22, Arg76, Gln77, and Ser44), and the communication network of these interactions provided insights into binding dynamics.</p>","PeriodicalId":22,"journal":{"name":"ACS Omega","volume":"10 22","pages":"22884–22908 22884–22908"},"PeriodicalIF":4.3000,"publicationDate":"2025-05-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.acs.org/doi/epdf/10.1021/acsomega.5c00053","citationCount":"0","resultStr":"{\"title\":\"Discovery and Exploration of Small Molecule Binders for CT83: Computational Insights from Homology Modeling, Virtual Screening, MD Simulations, Interaction Fingerprint, and Network Communications\",\"authors\":\"Varun Dewaker, Sung Taek Park, Jae Jun Lee* and Hyeong Su Kim*, \",\"doi\":\"10.1021/acsomega.5c0005310.1021/acsomega.5c00053\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >Kita-Kyushu lung cancer antigen-1 (KK-LC-1), also known as CT83, is a member of the cancer/testis antigen (CTA) family and has emerged as an important target for cancer therapy. 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引用次数: 0
摘要
kita -九州肺癌抗原-1 (KK-LC-1),也被称为CT83,是癌症/睾丸抗原(CTA)家族的一员,已成为癌症治疗的重要靶点。它的表达通常仅限于某些癌症,包括非小细胞肺癌、胃癌、三阴性乳腺癌和睾丸组织,这使它成为针对癌细胞的靶向药物开发的有吸引力的候选者。我们参考文献中报道的化合物Z839878730,通过PubChem化学性质搜索、Lipinski规则过滤、虚拟筛选、分子对接和分子动力学(MD)模拟,鉴定了几个新的小分子。所选分子为CID24326943、CID24459131、CID46375999、CID46533890和CID55836895。MD模拟(200 ns)显示了稳定的ct83 -配体配合物,MMPBSA计算显示Z839878730、CID24459131和CID46375999具有最有利的相对结合自由能。其中,CID46375999与参比化合物具有较大的相似性,具有1,3,4-噻二唑-2-羧酰胺支架,疏水性和氢键电位。相比之下,CID24459131具有咪唑烷酮环和相对较大的取代基,如二苯乙基部分,具有更灵活和扩展的构象。虽然CID46375999含有一个哌啶环,但与CID24459131相比,它的整体结构更受构象约束,这可能是由于可旋转键更少,结构更紧凑。总体而言,CID46375999在化学性质方面与参考化合物更接近。相互作用指纹图谱分析揭示了其与关键残基Leu15、Ile16、Phe18、Trp19、Arg22、Leu38、Arg42、Pro43、Arg76、Gln77和Ile80之间的频繁相互作用,包括疏水相互作用、π堆叠(Phe18和Trp19)和氢键(Arg22、Arg76、Gln77和Ser44),这些相互作用的通讯网络为其结合动力学提供了线索。
Discovery and Exploration of Small Molecule Binders for CT83: Computational Insights from Homology Modeling, Virtual Screening, MD Simulations, Interaction Fingerprint, and Network Communications
Kita-Kyushu lung cancer antigen-1 (KK-LC-1), also known as CT83, is a member of the cancer/testis antigen (CTA) family and has emerged as an important target for cancer therapy. Its expression is typically restricted to certain cancers, including nonsmall cell lung cancer, gastric cancer, triple-negative breast cancer, and testicular tissues, making it an attractive candidate for targeted drug development against cancer cells. We identified several new small molecules using PubChem chemical property searches, Lipinski rule-based filtration, virtual screening, molecular docking, and molecular dynamics (MD) simulations, with reference to the compound Z839878730 reported in the literature. The selected molecules were CID24326943, CID24459131, CID46375999, CID46533890, and CID55836895. MD simulations (200 ns) revealed stable CT83-ligand complexes, with MMPBSA calculations showing that Z839878730, CID24459131, and CID46375999 exhibited the most favorable relative binding free energies. Among these, CID46375999 shared greater similarity with the reference compound, featuring a 1,3,4-thiadiazole-2-carboxamide scaffold, hydrophobic properties, and hydrogen bonding potential. In contrast, CID24459131, which features an imidazolidinone ring and relatively bulky substituents such as a diphenylethyl moiety, exhibits a more flexible and extended conformation. Although CID46375999 contains a piperidine ring, its overall structure is more conformationally constrained compared to CID24459131, likely due to fewer rotatable bonds and a more compact architecture. Overall, CID46375999 aligned more closely with the reference compound in terms of chemical properties. Interaction fingerprint analysis revealed frequent interactions with key residues Leu15, Ile16, Phe18, Trp19, Arg22, Leu38, Arg42, Pro43, Arg76, Gln77, and Ile80, including hydrophobic interactions, π-stacking (Phe18 and Trp19), and H-bonds (Arg22, Arg76, Gln77, and Ser44), and the communication network of these interactions provided insights into binding dynamics.
ACS OmegaChemical Engineering-General Chemical Engineering
CiteScore
6.60
自引率
4.90%
发文量
3945
审稿时长
2.4 months
期刊介绍:
ACS Omega is an open-access global publication for scientific articles that describe new findings in chemistry and interfacing areas of science, without any perceived evaluation of immediate impact.