Computational Model to Predict Potential Therapeutic Targets Employing Generative Adversarial Networks for Analysis of Proteins Involved in Mycobacterium fortuitum Biofilm Formation.

IF 3.5 4区 医学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Current medicinal chemistry Pub Date : 2025-01-01 DOI:10.2174/0109298673345515241122024326
Shan Ghai, Rahul Shrivastava, Shruti Jain
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Abstract

A planktonic population of bacteria can form a biofilm by adhesion and colonization. Proteins known as "adhesins" can bind to certain environmental structures, such as sugars, which will cause the bacteria to attach to the substrate. Quorum sensing is used to establish the population is dense enough to form a biofilm. This paper presents a comprehensive overview of our investigation into these processes, specifically focusing on Mycobacterium fortuitum, an emerging pathogen of increasing clinical relevance. In our study, we detailed the methodology employed for the proteomic analysis of M. fortuitum, as well as our innovative application of Generative Adversarial Networks (GANs). These advanced computational tools allow us to analyze complex data sets and identify patterns that might otherwise remain obscured. With a particular focus on the effectiveness of GAN, the identified proteins and their potential roles in the context of M. fortuitum's pathogenesis were discussed. The insights gained from this study can significantly contribute to our understanding of this emerging pathogen and pave the way for developing targeted interventions, potentially leading to improved diagnostic tools and more effective therapeutic strategies against M. fortuitum infection. The authors achieved 95.43% accuracy for the generator and 87.89% for the discriminator. The model was validated by considering different Machine learning algorithms, reinforcing that integrating computational techniques with microbiological investigations can significantly enhance our understanding of emerging pathogens. Overall, this study emphasizes the importance of exploring the molecular mechanisms behind biofilm formation and pathogenicity, providing a foundation for future research that could lead to innovative solutions in combating infections caused by M. fortuitum and other similar pathogens.

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利用生成对抗网络预测潜在治疗靶点的计算模型,用于分析与偶然性分枝杆菌生物膜形成有关的蛋白质。
浮游菌群可以通过粘附和定植形成生物膜。被称为“粘附素”的蛋白质可以与特定的环境结构结合,比如糖,这将导致细菌附着在底物上。群体感应用于确定种群是否足够密集以形成生物膜。本文介绍了我们对这些过程的调查的全面概述,特别侧重于偶发分枝杆菌,一种日益临床相关性的新兴病原体。在我们的研究中,我们详细介绍了用于M. fortuitum蛋白质组学分析的方法,以及我们对生成对抗网络(gan)的创新应用。这些先进的计算工具使我们能够分析复杂的数据集,并识别出可能仍然模糊不清的模式。特别关注GAN的有效性,讨论了鉴定的蛋白质及其在福氏分枝杆菌发病机制中的潜在作用。从这项研究中获得的见解可以显著有助于我们对这种新兴病原体的理解,并为开发有针对性的干预措施铺平道路,可能导致改进诊断工具和更有效的治疗策略,以对抗幸运分枝杆菌感染。生成器和鉴别器的准确率分别达到95.43%和87.89%。该模型通过考虑不同的机器学习算法进行了验证,强调了将计算技术与微生物研究相结合可以显著提高我们对新兴病原体的理解。总之,本研究强调了探索生物膜形成和致病性背后的分子机制的重要性,为未来的研究提供了创新的解决方案,以对抗幸运分枝杆菌和其他类似病原体引起的感染奠定了基础。
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来源期刊
Current medicinal chemistry
Current medicinal chemistry 医学-生化与分子生物学
CiteScore
8.60
自引率
2.40%
发文量
468
审稿时长
3 months
期刊介绍: Aims & Scope Current Medicinal Chemistry covers all the latest and outstanding developments in medicinal chemistry and rational drug design. Each issue contains a series of timely in-depth reviews and guest edited thematic issues written by leaders in the field covering a range of the current topics in medicinal chemistry. The journal also publishes reviews on recent patents. Current Medicinal Chemistry is an essential journal for every medicinal chemist who wishes to be kept informed and up-to-date with the latest and most important developments.
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