Institute of Structural and Molecular Biology, Division of Biosciences, University College London, London, UK.
MAbs. 2022 Jan-Dec;14(1):2101183. doi: 10.1080/19420862.2022.2101183.
As interest in antibody-based drug development continues to increase, the biopharmaceutical industry has begun to focus on complex multi-specific antibodies (MsAbs) as an up-and-coming class of biologic that differ from natural monoclonal antibodies through their ability to bind to more than one type of antigen. As techniques to generate such molecules have diversified, so have their formats and the need for standard notation. Previous efforts to develop a notation language for macromolecule drugs have been insufficient, or too complex, for MsAbs. Here, we present Antibody Markup Language (AbML), a new notation language specifically for antibody formats that overcomes the limitations of existing languages and can annotate all current antibody formats, including fusions, fragments, standard antibodies and MsAbs, as well as all currently conceivable future formats. AbML V1.1 also provides explicit support for T-cell receptor domains. To assist users of this language we have also developed a tool, abYdraw, that can draw antibody schematics from AbML strings or generate an AbML string from a drawn antibody schematic. AbML has the potential to become a standardized notation for describing new MsAb formats entering clinical trials. AbML: Antibody Markup Language; ADC: Antibody-drug conjugate; CAS: Chemical Abstracts Service; CH: Constant heavy; CL: Constant light; Fv: Variable fragment; HELM: Hierarchical Editing Language for Macromolecules; HSA: Human serum albumin; INN: International Nonproprietary Names; KIH: Knobs-into-holes; mAbs: Monoclonal antibodies; MsAb: Multi-specific antibody; WHO: World Health Organization; PEG: Poly-ethylene glycol; scFv: Single-chain variable fragment; SMILES: Simplified Molecular-Input Line-Entry System; VH: Variable heavy; VHH: Single-domain (Camelid) variable heavy; VL: Variable light.
随着对抗体药物开发的兴趣不断增加,生物制药行业已开始关注复杂的多特异性抗体 (MsAbs),将其视为一种新兴的生物类药物,与通过结合多种类型的抗原来发挥作用的天然单克隆抗体不同。随着生成此类分子的技术多样化,它们的形式和对标准符号的需求也发生了变化。之前开发大分子药物符号语言的努力对于 MsAbs 来说不够充分或过于复杂。在这里,我们提出了抗体标记语言 (AbML),这是一种专门针对抗体形式的新符号语言,克服了现有语言的局限性,并可以注释所有当前的抗体形式,包括融合蛋白、片段、标准抗体和 MsAbs,以及所有当前可以想象的未来形式。AbML V1.1 还为 T 细胞受体结构域提供了明确的支持。为了帮助这种语言的使用者,我们还开发了一个工具 abYdraw,可以从 AbML 字符串绘制抗体示意图,或从绘制的抗体示意图生成 AbML 字符串。AbML 有可能成为描述进入临床试验的新型 MsAb 格式的标准化符号。AbML:抗体标记语言;ADC:抗体药物偶联物;CAS:化学文摘社;CH:恒定重链;CL:恒定轻链;Fv:可变片段;HELM:大分子层次编辑语言;HSA:人血清白蛋白;INN:国际非专利名称;KIH: knob-into-holes;mAbs:单克隆抗体;MsAb:多特异性抗体;WHO:世界卫生组织;PEG:聚乙二醇;scFv:单链可变片段;SMILES:简化分子输入行输入系统;VH:可变重链;VHH:单域(骆驼科)可变重链;VL:可变轻链。