IN SILICO STUDY OF CRYO-EM STRUCTURES OF ANTIGEN-ANTIBODY COMPLEX OF CHIKUNGUNYA FOR THE DEVELOPMENT OF DIAGNOSTIC AGENT

Authors

  • Toto Subroto Department of Pharmaceutical Analysis and Medicinal Chemistry, Faculty of Pharmacy, Universitas Padjadjaran, Indonesia
  • Rina Fajri Nuwarda Department of Chemistry, Faculty of Mathematics and Natural Sciences, Universitas Padjadjaran, Indonesia.
  • Umi Baroroh Department of Chemistry, Faculty of Mathematics and Natural Sciences, Universitas Padjadjaran, Indonesia.
  • Zuhrotun Nafisah Department of Chemistry, Faculty of Mathematics and Natural Sciences, Universitas Padjadjaran, Indonesia.
  • Bevi Lidya Doctoral Program in Biotechnology, School of Postgraduate Studies, Universitas Padjadjaran, Indonesia.
  • Muhammad Yusuf Department of Chemistry, Faculty of Mathematics and Natural Sciences, Universitas Padjadjaran, Indonesia.

DOI:

https://doi.org/10.22159/ajpcr.2017.v10s2.19489

Keywords:

Antibody, Chikungunya, in silico

Abstract

Objective: Despite the availability of the commercial rapid tests of chikungunya, the difference of pathogen's genotypes amongst different countries has created some causes for concern. It is found that the sensitivity of the current chikungunya rapid tests on Asian strain was only 20.5%, as compared to 90.3% when tested on the African phylogroup. Therefore, the development of diagnostics that is specific for the current strain circulating in the country is important to be done. The cryo-electron microscopy (cryo-EM) structures of antigen-antibody complex can be used as an insightful structural basis to the development of the tailored antibody for diagnostics purposes. However, cryo-EM structures usually were resolved in low resolution, thus some sterical clashes between residues are expected. This work aims to refine the cryo-EM structures of E1 E2 of chikungunya virus (CHIKV) in complex with antibody using molecular mechanics method, to calculate the binding energy of antigen-antibody complex, and to compare it with the experimental results.

Methods: Thecryo-EM structures were refined in vacuoby short minimization scheme using AMBER 14. The binding energies were calculated using Firedock and MM/GBSA methods.

Results:The results showed that the direct calculation of binding energies of cryo-EM structures reflected high repulsive forces. While the calculation on the refined structured showed lower binding energies. Visual inspections on the complex structures also indicated that the refined structures showed better interactions.

Conclusion:As a conclusion, the refinement of cryo-EM structures should be useful to gain more insight into the binding mode of interactions between antigenic protein and antibody, at the atomic level.

 

 

Downloads

Download data is not yet available.

References

Charrel R N, De Lamballerie X, Raoult D: Chikungunya Outbreaks - The Globalization of Vectorborne Diseases. N Engl J Med 2007; 356: 769-71.

Schwartz O, Albert ML: Biology and Pathogenesis of Chikungunya Virus. Nat Rev Micro 2010; 8: 491-500.

Sourisseau M, Schilte C, Casartelli N, Trouillet C, Guivel-Benhassine F, Rudnicka D, et al: Characterization of Reemerging Chikungunya Virus. PlosPathog 2007; 6: 804-17.

Burt FJ, Rolph, MS, Rulli NE, Mahalingam S, Heise MT: Chikungunya: A Re-Emerging Virus. Lancet 2012; 379: 662-71.

Pialoux G, Gaüzère BA, Jauréguiberry S, Strobel M: Chikungunya, an Epidemic Arbovirosis. Lancet Infect Dis 2007; 7: 319-27.

Kosasih H, De Mast Q, Widjaja S, Sudjana P, Antonjaya U, Ma'roef C, et al: Evidence for Endemic Chikungunya Virus Infections in Bandung, Indonesia. PlosNegl Trop Dis 2013; 7 Suppl10: e2483.

Kosasih H, Widjaja S, Surya E, Hadiwijaya SH, Butarbutar DP, Jaya UA, et al: Evaluation of Two IgM Rapid Immunochromatographic Tests during Circulation of Asian Lineage Chikungunya Virus. Southeast Asian J Trop Med Public Health 2012; 43 Suppl1: 55-61.

Sun S, Xiang Y., Akahata W, Holdaway H, Pal P, Zhang X, et al: Structural Analyses at Pseudo Atomic Resolution Of Chikungunya Virus and Antibodies Show Mechanisms of Neutralization. eLife 2013; 2: e00435.

Case DA, Babin V, Berryman JT, Betz RM, Cai Q, Cerutti DS: AMBER 14. University Of California, San Francisco; 2014

Andrusier N, Nussinov R, Wolfson HJ: Firedock: Fast Interaction Refinement in Molecular Docking. Proteins 2007; 69 Suppl 1: 139-59.

Miller III BR, Mcgee Jr TD, Swails JM, Homeyer N, Gohlke H, Roitberg AE: MMPBSA.py: An Efficient Program for End-State Free Energy Calculations. J ChemTheory Comput 2012; 8 Suppl 9: 3314-21.

Pal P, Dowd KA, Brien JD, Edeling MA, Gorlatov S, Johnson S, et al: Development of a Highly Protective Combination Monoclonal Antibody Therapy against Chikungunya Virus. PlosPathog 2013; 4: e1003312.

Liu Y, Liu Y, Mernaugh RL, Zeng X: Single Chain Fragment Variable Recombinant Antibody Functionalized Gold Nanoparticles for A Highly Sensitive Colorimetric Immunoassay. Biosensors and Bioelectronics 2009; 24: 2853–7.

Holstein CA, Chevalier A, Bennett S, Anderson CE, Keniston K, Olsen C, et al: Immobilizing Affinity Proteins to Nitrocellulose: A Toolbox for Paper-based Assay Developers. Anal BioanalChem 2016; 408: 1335 - 46

Wang J, Hou T, Xu X: Recent Advances in Free Energy Calculations with a Combination of Molecular Mechanics and Continuum Models. CurrComput Aided Drug Des 2006; 2: 95-103.

Published

01-05-2017

How to Cite

Subroto, T., R. F. Nuwarda, U. Baroroh, Z. Nafisah, B. Lidya, and M. Yusuf. “IN SILICO STUDY OF CRYO-EM STRUCTURES OF ANTIGEN-ANTIBODY COMPLEX OF CHIKUNGUNYA FOR THE DEVELOPMENT OF DIAGNOSTIC AGENT”. Asian Journal of Pharmaceutical and Clinical Research, vol. 10, no. 14, May 2017, pp. 62-64, doi:10.22159/ajpcr.2017.v10s2.19489.

Issue

Section

Original Article(s)