Computational Approach to Identify Potential Inhibitors against Multi-target Proteins of COVID-19 through Drug Repurposing

核心概念

A computational framework combining molecular docking and machine learning regression models can effectively identify potential inhibitors against the multi-target proteins of COVID-19, including Spike, 3CLpro, and Nucleocapsid.

摘要

This study proposes a computational framework to investigate potential inhibitors against COVID-19 through drug repurposing strategies. The framework consists of three key modules:

1. Data Preparation and Molecular Docking:

   • The study targets the Spike, 3CLpro, and Nucleocapsid proteins of SARS-CoV-2 as they are essential for viral entry, replication, and assembly.
   • A dataset of 5,903 approved drugs from the ZINC database was preprocessed and used for molecular docking against the target proteins.

2. QSAR Modeling:

   • Multiple machine learning regression models, including Decision Tree Regression (DTR), were developed to predict the binding affinities of the drug compounds towards the target proteins.
   • The DTR model outperformed other regression models, achieving R^2 values of 0.95, 0.97, and 0.93, and RMSE values of 1.66, 1.57, and 1.49 for Spike, 3CLpro, and Nucleocapsid, respectively, using the MACCS fingerprint feature set.

3. Molecular Docking and Drug Analysis:

   • The molecular docking analysis identified five promising drug candidates with binding affinities ranging from -19.7 to -12.6 kcal/mol.
   • The physicochemical properties of the selected drug candidates were analyzed to assess their potential efficacy and safety in biological systems.

The study demonstrates the effectiveness of the proposed computational framework in identifying potential COVID-19 inhibitors through drug repurposing, leveraging the combination of molecular docking and machine learning regression models. The findings provide a foundation for further in vitro and in vivo investigations to validate the identified drug candidates as potential COVID-19 therapeutics.

統計資料

The binding affinities (in kcal/mol) of the top five drug candidates towards the target proteins are:

ZINC003873365: -19.7 (Spike), -15.1 (3CLpro), -19.2 (Nucleocapsid)
ZINC085432544: -15.3 (Spike), -14.4 (3CLpro), -14.0 (Nucleocapsid)
ZINC085536956: -14.4 (Spike), -13.9 (3CLpro), -12.6 (Nucleocapsid)
ZINC008214470: -15.3 (Spike), -13.6 (3CLpro), -14.3 (Nucleocapsid)
ZINC261494640: -13.9 (Spike), -13.6 (3CLpro), -14.4 (Nucleocapsid)

引述

"Our findings with best scores of R2 and RMSE demonstrated that our proposed Decision Tree Regression (DTR) model is the most appropriate model to explore the potential inhibitors."
"We proposed five novel promising inhibitors with their respective Zinc IDs ZINC (3873365, 85432544, 8214470, 85536956, and 261494640) within the range of -19.7 kcal/mol to -12.6 kcal/mol."

從以下內容提煉的關鍵洞見

To Explore the Potential Inhibitors against Multitarget Proteins of COVID 19 using In Silico Study

by Imra Aqeel 於 arxiv.org 09-26-2024

https://arxiv.org/pdf/2409.16486.pdf

深入探究

What experimental validation steps would be necessary to confirm the efficacy of the identified drug candidates against COVID-19?

To confirm the efficacy of the identified drug candidates against COVID-19, a series of experimental validation steps are essential. These steps can be categorized into in vitro, in vivo, and clinical trials:

In Vitro Studies:

Cell Culture Assays: The first step involves testing the identified drug candidates in cell lines that are susceptible to SARS-CoV-2 infection. This includes using Vero E6 cells or human lung epithelial cells to assess the antiviral activity of the compounds. The drugs should be administered at various concentrations to determine their half-maximal inhibitory concentration (IC50).
Mechanism of Action Studies: Understanding how the drugs inhibit viral replication is crucial. This can involve assessing their effects on viral entry, replication, and assembly. Techniques such as qRT-PCR can be used to measure viral RNA levels post-treatment.

In Vivo Studies:

Animal Models: Following promising in vitro results, the next step is to evaluate the efficacy of the drug candidates in appropriate animal models, such as hamsters or mice that are infected with SARS-CoV-2. This will help assess the pharmacokinetics, optimal dosing, and potential side effects of the drugs.
Toxicity Studies: Evaluating the safety profile of the drug candidates is critical. This includes assessing any adverse effects on vital organs and overall health of the test subjects.

Clinical Trials:

Phase I Trials: These trials focus on safety and dosage in a small group of healthy volunteers. The primary goal is to determine the pharmacokinetics and pharmacodynamics of the drug candidates.
Phase II Trials: In this phase, the efficacy of the drug candidates is tested in a larger group of COVID-19 patients. The primary endpoints would include the reduction in viral load and improvement in clinical symptoms.
Phase III Trials: These trials involve a larger population and are designed to confirm the efficacy and monitor adverse reactions in a diverse patient population. The results from these trials will provide the necessary data for regulatory approval.

Post-Marketing Surveillance: After approval, ongoing monitoring of the drug's performance in the general population is essential to identify any long-term effects or rare adverse reactions.

How could the proposed computational framework be adapted to identify inhibitors for other viral diseases or health conditions beyond virology?

The proposed computational framework can be adapted to identify inhibitors for other viral diseases or health conditions by following these steps:

Target Identification:

The first step involves identifying key proteins or enzymes involved in the life cycle of the virus or disease of interest. This could include viral entry proteins, replication enzymes, or host cell receptors that the pathogen exploits.

Database Expansion:

The framework can utilize various chemical databases beyond the ZINC database, such as ChEMBL or PubChem, to screen a broader range of compounds. This would enhance the diversity of potential inhibitors.

Molecular Docking and QSAR Modeling:

The existing molecular docking and QSAR modeling techniques can be applied to new targets. By adjusting the input parameters and target proteins, the framework can predict binding affinities and interactions for different diseases.
Machine learning algorithms can be retrained with new datasets specific to the disease of interest, allowing for the identification of novel inhibitors based on structural similarities.

Integration of Multi-Omics Data:

Incorporating genomic, proteomic, and metabolomic data can provide insights into the disease mechanisms and potential drug targets. This holistic approach can enhance the predictive power of the computational framework.

Validation and Iteration:

The framework should include feedback loops where experimental validation results inform and refine the computational models. This iterative process will improve the accuracy of predictions for various diseases.

Application to Non-Viral Conditions:

The framework can also be adapted for non-viral diseases, such as cancer or metabolic disorders, by focusing on specific pathways or targets relevant to those conditions. The same principles of molecular docking and QSAR modeling can be applied to identify small molecules that modulate these pathways.

What potential synergistic effects could arise from combining the identified drug candidates with other COVID-19 treatments, and how could this be explored computationally?

Combining the identified drug candidates with other COVID-19 treatments could yield several potential synergistic effects, which can be explored through computational methods:

Enhanced Efficacy:

The identified drug candidates may target different stages of the viral life cycle compared to existing treatments (e.g., antivirals like remdesivir or protease inhibitors like paxlovid). This multi-target approach can lead to a more comprehensive inhibition of viral replication and spread.

Reduction of Resistance:

Using a combination of drugs can reduce the likelihood of viral resistance developing. By targeting multiple pathways, the virus may find it more challenging to adapt to the treatment.

Improved Clinical Outcomes:

Synergistic combinations may lead to faster recovery times and reduced severity of symptoms in patients. This can be particularly important for high-risk populations.

Computational Exploration:

Network Pharmacology: Utilizing network pharmacology approaches can help identify potential interactions between the identified drug candidates and existing COVID-19 treatments. This involves mapping out the biological pathways and networks affected by the drugs.
Molecular Docking Studies: Conducting molecular docking studies on combinations of drugs can provide insights into how they interact at the molecular level. This can help predict whether the combined drugs will enhance or inhibit each other's effects.
Machine Learning Models: Developing machine learning models that incorporate data from previous combination therapies can help predict the outcomes of new combinations. These models can analyze large datasets to identify patterns and potential synergistic effects.
In Silico Combination Screening: The computational framework can be adapted to perform virtual screening of drug combinations, assessing their binding affinities and potential interactions. This can prioritize combinations for further experimental validation.

Clinical Trial Design:

The insights gained from computational studies can inform the design of clinical trials for combination therapies, optimizing dosing regimens and patient selection to maximize therapeutic benefits.

By leveraging computational tools, researchers can efficiently explore the potential of drug combinations, paving the way for more effective treatment strategies against COVID-19 and other diseases.