Molecular Modeling and Affinity Determination of scFv Antibody: Proper Linker Peptide Enhances Its Activity
文献类型：期刊论文
| 作者 | Gu X; Jia XL(贾潇凌) ; Feng JN; Shen BF; Huang Y; Geng SS; Sun YX; Wang Y; Li Y; Long M(龙勉)
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| 刊名 | Annals of Biomedical Engineering
 |
| 出版日期 | 2010 |
| 卷号 | 38期号:2页码:537-549 |
| 通讯作者邮箱 | mlong@imech.ac.cn |
| 关键词 | Linker peptide Molecular modeling Micropipette adhesion frequency Scatchard analysis Binding affinity |
| ISSN号 | 0090-6964 |
| 通讯作者 | 龙勉 |
| 合作状况 | 国内 |
| 中文摘要 | One of existing strategies to engineer active antibody is to link VH and VL domains via a linker peptide. How the composition, length, and conformation of the linker affect antibody activity, however, remains poorly understood. In this study, a dual approach that coordinates molecule modeling, biological measurements, and affinity evaluation was developed to quantify the binding activity of a novel stable miniaturized anti-CD20 antibody or singlechain fragment variable (scFv) with a linker peptide. Upon computer-guided homology modeling, distance geometry analysis, and molecular superimposition and optimization, three new linker peptides PT1, PT2, and PT3 with respective 7, 10, and 15 residues were proposed and three engineered antibodies were then constructed by linking the cloned VH and VL domains and fusing to a derivative of human IgG1. The binding stability and activity of scFv-Fc chimera to CD20 antigen was quantified using a micropipette adhesion frequency assay and a Scatchard analysis. Our data indicated that the binding affinity was similar for the chimera with PT2 or PT3 and ~24-fold higher than that for the chimera with PT1, supporting theoretical predictions in molecular modeling. These results further the understanding in the impact of linker peptide on antibody structure and activity. |
| 学科主题 | 生物力学 |
| 类目[WOS] | Engineering, Biomedical |
| 研究领域[WOS] | Engineering |
| 关键词[WOS] | LIGAND BINDING-KINETICS ; SINGLE-CHAIN ANTIBODY ; ALKALINE-PHOSPHATASE ; CRYSTAL-STRUCTURE ; ESCHERICHIA-COLI ; FLOW-CYTOMETRY ; FV FRAGMENT ; CELL-CYCLE ; ANTIGEN ; DESIGN |
| 收录类别 | SCI |
| 语种 | 英语 |
| WOS记录号 | WOS:000274237000024 |
| 公开日期 | 2009-12-31 |
| 源URL | [http://dspace.imech.ac.cn/handle/311007/33025]  |
| 专题 | 力学研究所_国家微重力实验室 |
| 通讯作者 | Long M(龙勉) |
| 推荐引用方式 GB/T 7714 | Gu X,Jia XL,Feng JN,et al. Molecular Modeling and Affinity Determination of scFv Antibody: Proper Linker Peptide Enhances Its Activity[J]. Annals of Biomedical Engineering,2010,38(2):537-549. |
| APA | Gu X.,Jia XL.,Feng JN.,Shen BF.,Huang Y.,...&龙勉.(2010).Molecular Modeling and Affinity Determination of scFv Antibody: Proper Linker Peptide Enhances Its Activity.Annals of Biomedical Engineering,38(2),537-549. |
| MLA | Gu X,et al."Molecular Modeling and Affinity Determination of scFv Antibody: Proper Linker Peptide Enhances Its Activity".Annals of Biomedical Engineering 38.2(2010):537-549. |
入库方式： OAI收割
来源：力学研究所
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