Isolation and identification of the new baicalin target protein to develop flavonoid structure-based therapeutic agents

被引:2
作者
Kusakabe, Yoshio [1 ]
Moriya, Shun-Suke [1 ]
Sugiyama, Toru [1 ]
Miyata, Yoshiki [1 ]
机构
[1] Teikyo Univ, Fac Pharm Sci, Tokyo, Japan
关键词
Flavonoid target protein; Inhibition assay; In silico study; And cell biology; GLYCERALDEHYDE-3-PHOSPHATE DEHYDROGENASE; BINDING; GAPDH; MECHANISM; TRANSLOCATION; PURIFICATION; SCUTELLARIA; EXPRESSION; RECEPTOR; WOGONIN;
D O I
10.1016/j.bmc.2023.117362
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Proteins are vital constituents of all living organisms. As many therapeutic agents alter the activity of functional proteins, identifying functional target proteins of small bioactive molecules is essential for the rational design of stronger medicines. Flavonoids with antioxidant, anti-allergy, and anti-inflammatory effects are expected to have preventive effects for several diseases closely related to oxidation and inflammation, including heart disease, cancer, neurodegenerative disorders, and eye diseases. Therefore, identifying the proteins involved in the pharmacological actions of flavonoids, and designing a flavonoid structure-based medicine that strongly and specifically inhibits flavonoid target proteins, could aid the development of more effective medicines for treating heart disease, cancer, neurodegenerative disorders, and ocular diseases with few side effects. To isolate the flavonoid target protein, we conducted a novel affinity chromatography in a column wherein baicalin, a representative flavonoid, was attached to Affi-Gel 102. Through affinity chromatography and nano LC-MS/MS, we identified GAPDH as a flavonoid target protein. Then, we performed fluorescence quenching and an enzyme inhibition assay to experimentally confirm baicalin's binding affinity for, and inhibition of, GAPDH. We also conducted in silico docking simulations to visualize the binding modes of baicalin and the newly identified flavonoid target protein, GAPDH. From the results of this study, it was considered that one of the reasons why baicalin exhibits the effects on cancer and neurodegenerative diseases is that it inhibits the activity of GAPDH. In summary, we showed that Affi-Gel102 could quickly and accurately isolate the target protein for bioactive small molecules, without the need for isotopic labeling or a fluorescent probe. By using the method presented here, it was possible to easily isolate the target protein of a medicine containing a carboxylic acid.
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页数:11
相关论文
共 54 条
[1]   Baicalein Neutralizes Hypercholesterolemia-Induced Aggravation of Oxidative Injury in Rats [J].
AlSaad, Abdulaziz M. S. ;
Mohany, Mohamed ;
Almalki, Mohammed S. ;
Almutham, Ibrahim ;
Alahmari, Abdulwahab A. ;
AlSulaiman, Mohammed ;
Al-Rejaie, Salim S. .
INTERNATIONAL JOURNAL OF MEDICAL SCIENCES, 2020, 17 (09) :1156-1166
[2]   Baicalein: A review of its anti-cancer effects and mechanisms in Hepatocellular Carcinoma [J].
Bie, Beibei ;
Sun, Jin ;
Guo, Ying ;
Li, Jun ;
Jiang, Wei ;
Yang, Jun ;
Huang, Chen ;
Li, Zongfang .
BIOMEDICINE & PHARMACOTHERAPY, 2017, 93 :1285-1291
[3]   Natural Products and Their Biological Targets: Proteomic and Metabolomic Labeling Strategies [J].
Boettcher, Thomas ;
Pitscheider, Maximilian ;
Sieber, Stephan A. .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2010, 49 (15) :2680-2698
[4]   ISOLATION AND PURIFICATION OF MORPHINE RECEPTOR BY AFFINITY-CHROMATOGRAPHY [J].
CHO, TM ;
GE, BL ;
LOH, HH .
LIFE SCIENCES, 1985, 36 (11) :1075-1085
[5]   Novel roles for GAPDH in cell death and carcinogenesis [J].
Colell, A. ;
Green, D. R. ;
Ricci, J-E .
CELL DEATH AND DIFFERENTIATION, 2009, 16 (12) :1573-1581
[6]   Molecular recognition of bio-active flavonoids quercetin and rutin by bovine hemoglobin: an overview of the binding mechanism, thermodynamics and structural aspects through multi-spectroscopic and molecular dynamics simulation studies [J].
Das, Sourav ;
Bora, Nikita ;
Rohman, Mostofa Ataur ;
Sharma, Raju ;
Jha, Anupam Nath ;
Roy, Atanu Singha .
PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2018, 20 (33) :21668-21684
[7]   MICROTUBULES BIND GLYCERALDEHYDE-3-PHOSPHATE DEHYDROGENASE AND MODULATE ITS ENZYME-ACTIVITY AND QUATERNARY STRUCTURE [J].
DURRIEU, C ;
BERNIERVALENTIN, F ;
ROUSSET, B .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1987, 252 (01) :32-40
[8]   AN IMMUNOLOGICAL STUDY OF BAND-3, THE ANION TRANSPORT PROTEIN OF THE HUMAN RED-BLOOD-CELL MEMBRANE [J].
ENGLAND, BJ ;
GUNN, RB ;
STECK, TL .
BIOCHIMICA ET BIOPHYSICA ACTA, 1980, 623 (01) :171-182
[9]   Mechanism-based profiling of enzyme families [J].
Evans, Michael J. ;
Cravatt, Benjamin F. .
CHEMICAL REVIEWS, 2006, 106 (08) :3279-3301
[10]   PURIFICATION AND PROPERTIES OF UROPORPHYRINOGEN DECARBOXYLASE FROM SACCHAROMYCES-CEREVISIAE - YEAST UROPORPHYRINOGEN DECARBOXYLASE [J].
FELIX, F ;
BROUILLET, N .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1990, 188 (02) :393-403