连接器
结合
计算机科学
有效载荷(计算)
编码器
组合化学
相容性(地球化学)
独特性
化学
生成模型
共轭梯度法
计算生物学
解码方法
序列(生物学)
算法
合理设计
极地的
生成语法
编码(内存)
理论计算机科学
人工智能
财产(哲学)
作者
Yanjing Chen,Fanhong Wu,Yiwei Liu,Yichu Wu,Dong Wang,Jingjing Wu
标识
DOI:10.1021/acs.jcim.6c01342
摘要
The rational generation of antibody-drug conjugate (ADC) linkers remains challenging due to the need to balance linker stability, payload release, and compatibility with antibody-payload components. We propose MolT5-Linker, a Transformer-based generative framework conditioned on antibody sequences and payload molecular structures. In the encoder stage, the model integrates a GAT-based Attachment Site Attention Network that infers putative attachment sites from antibody and payload representations. This site-related information guides the decoder to generate chemically compatible linker candidates, improving compatibility between generated linkers and ADC components. Following fine-tuning on a self-constructed ADC data set, MolT5-Linker achieves a generation validity of 0.8986 while maintaining a balance between molecular recovery (0.5802) and uniqueness (0.5438). Furthermore, the generated linker candidates exhibit medicinal chemistry property distributions─including molecular weight, lipophilicity, and topological polar surface area (TPSA)─consistent with ground-truth ADC linkers. These results highlight MolT5-Linker as a computational framework for ADC linker candidate generation.
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