Measuring and locating the changes in protein structure using MELO

Understanding the impact that subtle variations (missense mutation, environmental change, ion chelation, ligand binding, etc.) have on protein structure helps to reveal their biological effects, but remain extremely challenging due to the difficulty in measuring and locating the changes in protein structure. Herein, a method entitled MELO is therefore constructed, which enable a systematic measurement based on residues' geometric characteristics & relative distance and a high-throughput location of structural change based on secondary structure variation & protein segment shift. Our method performs best in capturing the structure changes of various degrees of magnitude (some increases were >30%) and is capable of precisely locating the regions of alterations for critical case studies. Moreover, it identifies over 10,000 structural changes induced by subtle variation that existing methods fail to detect. An online server allows users to upload their structures for comparison, and all those structural changes identified in this study have also been made available for download.

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Publication Details

Journal
Nature Communications
Published
2026-01-05
DOI
https://doi.org/10.1038/s41467-025-68110-8
Primary Topic
Protein Structure and Dynamics
Type
article
Field-Weighted Citation Impact
0.00

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article

Measuring and locating the changes in protein structure using MELO

Tommy Fu, Minjie Mou, Yintao Zhang, Huaicheng Sun et al.
Nature Communications
Protein Structure and Dynamics
article

Measuring and locating the changes in protein structure using MELO

Tommy Fu, Minjie Mou, Yintao Zhang, Huaicheng Sun, Yang Liao, Haibin Dai, Lingyan Zheng, Xiuna Sun, Shuiyang Shi, Mingxuan Liu, Mingkun Lu, Feng Zhu, Chengbin Gu
article en

Abstract

Understanding the impact that subtle variations (missense mutation, environmental change, ion chelation, ligand binding, etc.) have on protein structure helps to reveal their biological effects, but remain extremely challenging due to the difficulty in measuring and locating the changes in protein structure. Herein, a method entitled MELO is therefore constructed, which enable a systematic measurement based on residues' geometric characteristics & relative distance and a high-throughput location of structural change based on secondary structure variation & protein segment shift. Our method performs best in capturing the structure changes of various degrees of magnitude (some increases were >30%) and is capable of precisely locating the regions of alterations for critical case studies. Moreover, it identifies over 10,000 structural changes induced by subtle variation that existing methods fail to detect. An online server allows users to upload their structures for comparison, and all those structural changes identified in this study have also been made available for download.

Nature CommunicationsVol. 17(1)
Sir Run Run Shaw Hospital (CN), Zhejiang Lab (CN), Second Affiliated Hospital of Zhejiang University (CN), Zhejiang University-University of Edinburgh Institute (CN), Alibaba Group (China) (CN), Zhejiang University (CN)
National Natural Science Foundation of China, Zhejiang University
Life in Land
Openalex Percentile: Top 97%
Protein Structure and Dynamics
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Measuring and locating the changes in protein structure using MELO — Tommy Fu, Minjie Mou, et al. · Nature Communications (2026) | TGRS Research Map | TGRS