Solubility and Stability Engineering of Human VH Domains
Solubility and stability are amongst the factors contributing to the therapeutic efficacy of biologics. Human antibody heavy chain variable domains, VHs, are one class of biologics; improving VH biophysical properties is the focus of significant protein engineering efforts. Here, we describe an efficacy engineering approach which involves the introduction of a disulfide linkage in the VH core and which improves both VH solubility and stability. More specifically, we describe protocols for generation of disulfide engineered human VHs and their characterization in terms of disulfide linkage formation, non-aggregation, and stability. Our solubility/stability engineering approach may be applied to other VHs.
- 基本防御屏障和生理防御屏障
- 體細胞高頻突變形成免疫球蛋白的多樣性
- 條件性基因敲除的基本原理Cre/loxP重組系統
- 與HLAⅡ類抗原關聯的疾病
- 白介素12的生物學特性總結和受體通路圖
- Screening for Host Proteins with Pro- and Antiviral Activity Using High-Throughput RNAi
- Screening an Expression Library with a DNA Binding Site
- Monoclonal Antibodies to Chemokine Receptors
- Generation of Short-Term Murine Natural Killer Cell Clones to Analyze Ly49 Gene Expression
- Chromosomal Mapping of Genes by Nonisotopic In Situ Hybridization