Previous Drug Design methods and why we need the novel method QADD<\/h2>\n\n\n\n
Drug discovery initiates with the generation of potential drug candidates. Due to inefficient and deficient exploration of the chemical space, many potential drug candidates remain unmined, thereby limiting the number of molecules deposited in databases. A large number of potential drug-like molecules remain undiscovered as a consequence. The ChEMBL database houses approximately two million bioactive molecules with drug-like properties, of which the FDA has approved only 43,264 as drugs. This calls for method development for novel drug design that covers the chemical space extensively.<\/p>\n\n\n\n
Wet laboratory experiments for novel drug discovery are time-consuming, and with the advent of technology and high-performance computing, a plethora of computational<\/a> methods for drug design and discovery have been developed. Such methods include REINVENT<\/a>, MolGAN<\/a>, and others implementing deep learning<\/a> techniques for molecule generation with desired properties. <\/p>\n\n\n\n These deep learning methods can be broadly classified into two categories. The first group of methods uses deep generative models<\/a> to learn the distribution of the training molecules and generates similar novel molecules. An Auto-Encoder-Decoder based method uses the SMILES format to propose new molecules into a low -dimensional latent space using the Encoder and then samples molecules from the latent space and reconstructs molecules using the Decoder as <\/strong>demonstrated by Blaschke et al<\/a>. The General Adversarial Networks (GANs) comprise a generator network and a discriminator network and have been used in MolGAN<\/a> to propose molecular graphs. The generator outputs a molecular graph from a feature vector sampled with a prior, and the discriminator determines if the graph is from the training set or the generator. Methods implementing bidirectional recurrent neural networks<\/a> (BiRNNs) have also been developed by Grisoni et al<\/a>. <\/p>\n\n\n\n The second group of methods is based on optimizing objective functions derived from a combination of multiple properties. These methods are typically based on the Reinforcement learning paradigm, given the good optimization and exploration abilities of the methodology. Such methods include ReLeaSE<\/a>. These methods typically use a weighted combination of objective functions rendering a dominant objective function. Also, such methods are limited by the fact some high potential drug-like molecules are ignored as they do not meet these optimized properties. Thus, an effective Quality Assessment module is required for assessing the potential of drug-like molecules. Hence, with these limitations in mind, the authors developed QADD (Quality Assessment-based Drug Design), an iterative refinement framework combining a multi-objective deep reinforcement learning generator with a novel QA discriminator for de novo<\/em> drug discovery<\/a>.<\/p>\n\n\n\n The QADD pipeline involves the following steps:<\/p>\n\n\n\n The following figure illustrates the QADD pipeline.<\/p>\n\n\n The QADD methodology avoids information loss by optimizing multiple objective functions in parallel. The molecular QA module effectively discriminates and learns the distribution of molecules with high drug potential. The authors also generate molecules with high binding affinity to DRD2( Dopamine receptor type2). This is achieved using a binding prediction model designed to score target-specific binding affinity as one reward function of QADD. This module can be used to generate novel molecules for any biological targets.<\/p>\n\n\n\n The novel drug design methodology, QADD, is a game changer in the drug design and development field. It combines a reinforcement learning-based generator model with a molecular QA model discriminator in a synergistic way for generating de novo <\/em>molecules as potential drug molecules. The GNN-based novel QA module ensures the generation of high potential drug molecules. The iterative refinement framework improves the quality<\/em> of the molecules iteratively. The high efficacy of the method, coupled with the ability to span a greater scope of the chemical space, renders it as a groundbreaking method that will aid in the discovery of novel drug-like molecules and advance the development of better therapeutics. The ability of the method to generate molecules with high binding affinity for DRD2 also opens doors to finding such molecules for other biological molecules of interest as targets, thereby contributing significantly to drug design, development, and delivery.<\/p>\n\n\n\n Article Source: Reference Paper<\/a><\/p>\n\n\n\n Learn More:<\/mark><\/em><\/strong><\/p>\n\n\n\nA brief overview of the method QADD: Quality Assessment-based Drug Design<\/h2>\n\n\n\n
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![\"Enhancing\u00a0de](\"https:\/\/cbirt.net\/staging\/wp-content\/uploads\/2023\/04\/QADD.png\")
Image source: <\/em>https:\/\/doi.org\/10.1093\/bioinformatics\/btad157<\/figcaption><\/figure>\n<\/div>\n\n\nGenerating novel molecules with high binding affinity to DRD2<\/h2>\n\n\n\n
Conclusion<\/h2>\n\n\n\n