The three-dimensional structure of a protein underpins its biological function, making structure determination and prediction central challenges in structural biology. Although experimental techniques such as X-ray crystallography, nuclear magnetic resonance (NMR), and cryo-electron microscopy (cryo-EM) can yield high-resolution structures, they are limited by low throughput, high cost, and demanding sample preparation. Likewise, traditional computational methods often perform poorly in the absence of homologous templates or under complex folding dynamics. Recent advances in deep learning and large-scale protein language models have transformed protein structure prediction. Models such as AlphaFold3 and RoseTTAFold achieve near-experimental accuracy by integrating evolutionary information, geometric constraints, and end-to-end neural architectures, while single-sequence approaches such as ESMFold offer substantial gains in speed and scalability. This review summarizes the biochemical foundations of protein folding, recent AI-driven methodological advances, and representative applications in drug discovery, enzyme engineering, and disease research, and discusses current challenges and future directions.
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Tianxiang Yin
Yunxuan Chen
Yuhang Wang
SHILAP Revista de lepidopterología
Frontiers in Molecular Biosciences
University of Cincinnati
Hong Kong Polytechnic University
Xi'an Jiaotong University
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Yin et al. (Mon,) studied this question.
www.synapsesocial.com/papers/69b3aaa802a1e69014ccb70e — DOI: https://doi.org/10.3389/fmolb.2026.1767821