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Structural and functional alterations of myoglobin by glucose-protein interactions

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成果类型:
期刊论文
作者:
You, Yong;Liu, Fang;Du, Ke-Jie;Wen, Ge-Bo;Lin, Ying-Wu*
通讯作者:
Lin, Ying-Wu
作者机构:
[Wen, Ge-Bo; You, Yong; Liu, Fang] Univ South China, Inst Cardiovasc Dis, Hengyang 421001, Peoples R China.
[Wen, Ge-Bo; You, Yong; Liu, Fang] Univ South China, Key Lab Arteriosclerol Human Prov, Hengyang 421001, Peoples R China.
[Lin, Ying-Wu; Du, Ke-Jie] Univ South China, Sch Chem & Chem Engn, Hengyang 421001, Peoples R China.
[Wen, Ge-Bo; Lin, Ying-Wu] Univ South China, Lab Prot Struct & Funct, Hengyang 421001, Peoples R China.
通讯机构:
[Lin, Ying-Wu] U
Univ South China, Sch Chem & Chem Engn, Hengyang 421001, Peoples R China.
语种:
英文
关键词:
Diabetes;Heme protein;Glucose;Myoglobin;Peroxidase
期刊:
Journal of Molecular Modeling
ISSN:
1610-2940
年:
2014
卷:
20
期:
7
页码:
2358
基金类别:
NSFCNational Natural Science Foundation of China (NSFC) [31370812]; Scientific Research Foundation for the Returned Overseas Chinese Scholars, State Education MinistryScientific Research Foundation for the Returned Overseas Chinese Scholars; National Natural Science Foundation of ChinaNational Natural Science Foundation of China (NSFC)
机构署名:
本校为第一且通讯机构
院系归属:
化学化工学院
医学院
摘要:
The interaction of blood glucose with heme proteins plays a key role in inducing diabetes, a serious disease threatening human health. In this study, we investigated the non-covalent interaction between glucose and myoglobin (Mb), both theoretically and experimentally, using molecular dynamics (MD) simulation combined with spectroscopic studies. It revealed that glucoses can occupy the side pocket of Mb, and bind closely to one of the xenon cavities in Mb, by hydrogen bonding interactions with two propionate groups of heme as well as surrounding amino acids. These interactions alter the confor...

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