Evaluation of DNA-protein complex structures using the deep learning method.
Chengwei ZengYiren JianChen ZhuoAnbang LiChen ZengYunjie ZhaoPublished in: Physical chemistry chemical physics : PCCP (2023)
Biological processes such as transcription, repair, and regulation require interactions between DNA and proteins. To unravel their functions, it is imperative to determine the high-resolution structures of DNA-protein complexes. However, experimental methods for this purpose are costly and technically demanding. Consequently, there is an urgent need for computational techniques to identify the structures of DNA-protein complexes. Despite technological advancements, accurately identifying DNA-protein complexes through computational methods still poses a challenge. Our team has developed a cutting-edge deep-learning approach called DDPScore that assesses DNA-protein complex structures. DDPScore utilizes a 4D convolutional neural network to overcome limited training data. This approach effectively captures local and global features while comprehensively considering the conformational changes arising from the flexibility during the DNA-protein docking process. DDPScore consistently outperformed the available methods in comprehensive DNA-protein complex docking evaluations, even for the flexible docking challenges. DDPScore has a wide range of applications in predicting and designing structures of DNA-protein complexes.
Keyphrases
- circulating tumor
- protein protein
- single molecule
- high resolution
- cell free
- deep learning
- convolutional neural network
- small molecule
- molecular dynamics
- binding protein
- nucleic acid
- molecular dynamics simulations
- machine learning
- mass spectrometry
- transcription factor
- electronic health record
- artificial intelligence
- data analysis
- liquid chromatography