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发表于 2021-10-6 17:59:26
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本帖最后由 青龙偃月刀 于 2021-10-6 18:16 编辑
蛋白表达和纯化:合成PD-L1(19-134位)基因,C末端加入6his的融合蛋白标签T,插入到pET21b构建原核表达载体。
vHH HZ-C-Ye-18纳米抗体基因和人IgG1-FC端进行融合,插入到pcDNA3.1构建真核表达载体。
ExpiCHO表达细胞用于表达VHH抗体,用Protein A进行纯化,纯化后的vHH用IdeS进行酶切处理,用Protein G进行纯化,去除Fc段。再用GingisKHAN对vHH蛋白进行酶切,获得HZ-C-Ye-18. 4-1BB (25-162) 。同样的方法制备得到另一株纳米抗体HZ-L-Yr-16
However, a truncated Fc with only Leu-Gly-Gly in the hinge region was cloned into the vector.23 The encoded plasmid was transiently transfected into Expi293 cells (Life technologies) using polyethylenimine (PEI). For 4-1BB, the eluted protein was concentrated, cleaved by IdeS and purified by a Protein A column. The 4-1BB monomer was separated from 4-1BB homodimer using on a Superdex 75 Increase 10/300 GL column. For HZ-LYr-16, only one step purification was performed using a Protein G column after IdeS cleavage.
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