Complexation process and binding parameters of curcumin and short amylose with V7-type helix structure
Pre-formed V7-type short amylose (SA) could interact with curcumin to form inclusion complex (IC) thereby to improve the stability of curcumin. However, the complexation mechanism of V7-type SA and curcumin is not clear, which limit the improvement of inclusion efficiency. To obtain a starch nanocar...
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KeAi Communications Co., Ltd.
2024-12-01
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| Series: | Grain & Oil Science and Technology |
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| Online Access: | http://www.sciencedirect.com/science/article/pii/S2590259824000530 |
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| author | Xiaojing Li Lei Dai Jie Zhong Tingting Li Gongjian Fan Dandan Zhou Caie Wu |
| author_facet | Xiaojing Li Lei Dai Jie Zhong Tingting Li Gongjian Fan Dandan Zhou Caie Wu |
| author_sort | Xiaojing Li |
| collection | DOAJ |
| description | Pre-formed V7-type short amylose (SA) could interact with curcumin to form inclusion complex (IC) thereby to improve the stability of curcumin. However, the complexation mechanism of V7-type SA and curcumin is not clear, which limit the improvement of inclusion efficiency. To obtain a starch nanocarrier with high loading capacity, the encapsulation process and interaction parameters of V7-type SA-curcumin IC was studied. The analysis results demonstrated that stoichiometric ratio value of the SA-curcumin complex was around 1. V7-type SA performed excellently in the delivery of curcumin attributing to their high loading capacity (over 20%). It was found that curcumin could enter into the pre-formed helical cavity of SA to form an IC. The conformation change of SA caused the reduction in the interaction ratio in the last 20 ns of simulation. However, SA and curcumin always remained complexation status during the simulation. Hydrogen bonds (H-bonds) and hydrophobic interaction were the most critical acting forces involved in the formation and stability of V7-type SA-curcumin complex. Molecular docking presented that H-bonds interaction between curcumin ligand and V7-type SA chain (O3 at the 25th glucose unit, and O6 at the 17th and 20th glucose units) were found. Furthermore, the hydrophobic interactions were discovered between curcumin ligand and SA chain (18th, 19th, 21st, 22nd and 23rd glucose units). |
| format | Article |
| id | doaj-art-a46d8575c52a476aa7b73516381dcc1a |
| institution | OA Journals |
| issn | 2590-2598 |
| language | English |
| publishDate | 2024-12-01 |
| publisher | KeAi Communications Co., Ltd. |
| record_format | Article |
| series | Grain & Oil Science and Technology |
| spelling | doaj-art-a46d8575c52a476aa7b73516381dcc1a2025-08-20T02:34:19ZengKeAi Communications Co., Ltd.Grain & Oil Science and Technology2590-25982024-12-017424625310.1016/j.gaost.2024.09.001Complexation process and binding parameters of curcumin and short amylose with V7-type helix structureXiaojing Li0Lei Dai1Jie Zhong2Tingting Li3Gongjian Fan4Dandan Zhou5Caie Wu6Co-Innovation Center for the Sustainable Forestry in Southern China, Co-Innovation Center of Efficient Processing and Utilization of Forest Resources, Department of Food Science and Engineering, College of Light Industry and Food Engineering, Nanjing Forestry University, Nanjing, Jiangsu 210037, ChinaCollege of Food Science and Engineering, Qingdao Agricultural University, Shandong 266109, ChinaCo-Innovation Center for the Sustainable Forestry in Southern China, Co-Innovation Center of Efficient Processing and Utilization of Forest Resources, Department of Food Science and Engineering, College of Light Industry and Food Engineering, Nanjing Forestry University, Nanjing, Jiangsu 210037, ChinaCo-Innovation Center for the Sustainable Forestry in Southern China, Co-Innovation Center of Efficient Processing and Utilization of Forest Resources, Department of Food Science and Engineering, College of Light Industry and Food Engineering, Nanjing Forestry University, Nanjing, Jiangsu 210037, ChinaCo-Innovation Center for the Sustainable Forestry in Southern China, Co-Innovation Center of Efficient Processing and Utilization of Forest Resources, Department of Food Science and Engineering, College of Light Industry and Food Engineering, Nanjing Forestry University, Nanjing, Jiangsu 210037, ChinaCo-Innovation Center for the Sustainable Forestry in Southern China, Co-Innovation Center of Efficient Processing and Utilization of Forest Resources, Department of Food Science and Engineering, College of Light Industry and Food Engineering, Nanjing Forestry University, Nanjing, Jiangsu 210037, ChinaCo-Innovation Center for the Sustainable Forestry in Southern China, Co-Innovation Center of Efficient Processing and Utilization of Forest Resources, Department of Food Science and Engineering, College of Light Industry and Food Engineering, Nanjing Forestry University, Nanjing, Jiangsu 210037, China; Corresponding author.Pre-formed V7-type short amylose (SA) could interact with curcumin to form inclusion complex (IC) thereby to improve the stability of curcumin. However, the complexation mechanism of V7-type SA and curcumin is not clear, which limit the improvement of inclusion efficiency. To obtain a starch nanocarrier with high loading capacity, the encapsulation process and interaction parameters of V7-type SA-curcumin IC was studied. The analysis results demonstrated that stoichiometric ratio value of the SA-curcumin complex was around 1. V7-type SA performed excellently in the delivery of curcumin attributing to their high loading capacity (over 20%). It was found that curcumin could enter into the pre-formed helical cavity of SA to form an IC. The conformation change of SA caused the reduction in the interaction ratio in the last 20 ns of simulation. However, SA and curcumin always remained complexation status during the simulation. Hydrogen bonds (H-bonds) and hydrophobic interaction were the most critical acting forces involved in the formation and stability of V7-type SA-curcumin complex. Molecular docking presented that H-bonds interaction between curcumin ligand and V7-type SA chain (O3 at the 25th glucose unit, and O6 at the 17th and 20th glucose units) were found. Furthermore, the hydrophobic interactions were discovered between curcumin ligand and SA chain (18th, 19th, 21st, 22nd and 23rd glucose units).http://www.sciencedirect.com/science/article/pii/S2590259824000530Short amylosePre-formed helixCurcuminBinding affinityInteraction sites |
| spellingShingle | Xiaojing Li Lei Dai Jie Zhong Tingting Li Gongjian Fan Dandan Zhou Caie Wu Complexation process and binding parameters of curcumin and short amylose with V7-type helix structure Grain & Oil Science and Technology Short amylose Pre-formed helix Curcumin Binding affinity Interaction sites |
| title | Complexation process and binding parameters of curcumin and short amylose with V7-type helix structure |
| title_full | Complexation process and binding parameters of curcumin and short amylose with V7-type helix structure |
| title_fullStr | Complexation process and binding parameters of curcumin and short amylose with V7-type helix structure |
| title_full_unstemmed | Complexation process and binding parameters of curcumin and short amylose with V7-type helix structure |
| title_short | Complexation process and binding parameters of curcumin and short amylose with V7-type helix structure |
| title_sort | complexation process and binding parameters of curcumin and short amylose with v7 type helix structure |
| topic | Short amylose Pre-formed helix Curcumin Binding affinity Interaction sites |
| url | http://www.sciencedirect.com/science/article/pii/S2590259824000530 |
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