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使用免疫信息学和计算方法设计针对胆囊癌的基于肽的多表位疫苗构建体。

Designing of Peptide Based Multi-Epitope Vaccine Construct against Gallbladder Cancer Using Immunoinformatics and Computational Approaches.

作者信息

Dar Mukhtar Ahmad, Kumar Pawan, Kumar Prakash, Shrivastava Ashish, Dar Muneer Ahmad, Chauhan Richa, Trivedi Vinita, Singh Ashutosh, Khan Eshan, Velayutham Ravichandiran, Dhingra Sameer

机构信息

Department of Pharmacy Practice, National Institute of Pharmaceutical Education and Research (NIPER), Hajipur 844102, India.

Department of Biotechnology, National Institute of Pharmaceutical Education and Research (NIPER), Hajipur 844102, India.

出版信息

Vaccines (Basel). 2022 Oct 31;10(11):1850. doi: 10.3390/vaccines10111850.

Abstract

Gallbladder cancer (GBC) is an aggressive and difficult to treat biliary tract carcinoma with a poor survival rate. The aim of this study was to design a peptide-based multi-epitope vaccine construct against GBC using immunoinformatics approaches. Three proteins implicated in the progression of GBC were selected for B and T cell epitope prediction and the designing of the potential vaccine construct. Seven CTL, four HTL and six Bcell epitopes along with a suitable adjuvant were selected and connected using linkers for designing the vaccine construct. The secondary and tertiary models of the designed vaccine were generated and satisfactorily validated. A Ramachandran plot of the final 3D model showed more than 90% of the residues in allowed regions and only 0.4% in disallowed regions. The binding affinity of a vaccine construct with TLR 2, 3 and 4 receptors was assessed through molecular docking and simulation. The average numbers of hydrogen bonds for vaccine-TLR 2, 3 and 4 complexes in the simulation were 15.36, 16.45, and 11.98, respectively, and remained consistent over a 100 ns simulation period, which is critical for their function. The results of this study provide a strong basis for further evaluation through in vitro/in vivo experimental validation of the safety and efficacy of the designed vaccine construct.

摘要

胆囊癌(GBC)是一种侵袭性强且难以治疗的胆道癌,生存率很低。本研究的目的是使用免疫信息学方法设计一种针对胆囊癌的基于肽的多表位疫苗构建体。选择了三种与胆囊癌进展相关的蛋白质进行B细胞和T细胞表位预测以及潜在疫苗构建体的设计。选择了七个细胞毒性T淋巴细胞(CTL)表位、四个辅助性T淋巴细胞(HTL)表位和六个B细胞表位,并使用接头连接起来以设计疫苗构建体。生成了所设计疫苗的二级和三级模型,并进行了令人满意的验证。最终三维模型的拉氏图显示,超过90%的残基位于允许区域,只有0.4%位于禁止区域。通过分子对接和模拟评估了疫苗构建体与Toll样受体2(TLR 2)、TLR 3和TLR 4的结合亲和力。在模拟中,疫苗与TLR 2、TLR 3和TLR 4复合物的氢键平均数量分别为15.36、16.45和11.98,并且在100纳秒的模拟期内保持一致,这对它们的功能至关重要。本研究结果为通过体外/体内实验验证所设计疫苗构建体的安全性和有效性进行进一步评估提供了有力依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b8f4/9696659/0ae7a34c66d7/vaccines-10-01850-g001.jpg

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