Yuan Zhefan, McMullen Patrick, Luozhong Sijin, Sarker Pranab, Tang Chenjue, Wei Tao, Jiang Shaoyi
Meinig School of Biomedical Engineering, Cornell University Ithaca NY 14853 USA
Department of Chemical Engineering, Howard University Washington D.C. 20059 USA
Chem Sci. 2023 Jan 30;14(8):2033-2039. doi: 10.1039/d2sc07047b. eCollection 2023 Feb 22.
Antibodies against poly(ethylene glycol) (PEG) have been found to be the culprit of side reactions and efficacy loss of a number of PEGylated drugs. Fundamental mechanisms of PEG immunogenicity and design principles for PEG alternatives still have not been fully explored. By using hydrophobic interaction chromatography (HIC) under varied salt conditions, we reveal the "hidden" hydrophobicity of those polymers which are generally considered as hydrophilic. A correlation between the hidden hydrophobicity of a polymer and its polymer immunogenicity is observed when this polymer is conjugated with an immunogenic protein. Such a correlation of hidden hydrophobicity immunogenicity for a polymer also applies to corresponding polymer-protein conjugates. Atomistic molecular dynamics (MD) simulation results show a similar trend. Based on polyzwitterion modification and with this HIC technique, we are able to produce extremely low-immunogenic protein conjugates as their hydrophilicity is pushed to the limit and their hydrophobicity is eliminated, breaking the current barriers of eliminating anti-drug and anti-polymer antibodies.
聚乙二醇(PEG)抗体已被发现是多种聚乙二醇化药物发生副作用和疗效丧失的罪魁祸首。PEG免疫原性的基本机制以及PEG替代物的设计原则仍未得到充分探索。通过在不同盐条件下使用疏水相互作用色谱法(HIC),我们揭示了那些通常被认为是亲水性聚合物的“隐藏”疏水性。当这种聚合物与免疫原性蛋白偶联时,观察到聚合物的隐藏疏水性与其聚合物免疫原性之间存在相关性。聚合物的这种隐藏疏水性-免疫原性相关性也适用于相应的聚合物-蛋白偶联物。原子分子动力学(MD)模拟结果显示出类似趋势。基于聚两性离子修饰并使用这种HIC技术,我们能够生产出免疫原性极低的蛋白偶联物,因为它们的亲水性被推到极限且疏水性被消除,突破了目前消除抗药物和抗聚合物抗体的障碍。