克隆(Java方法)
生物
分子生物学
抗体
转铁蛋白受体
荧光显微镜
融合蛋白
病毒学
单克隆抗体
细胞生物学
内皮蛋白C受体
遗传学
噬菌体展示
表位
人脑
荧光
受体
重组DNA
基因
作者
Muhammad Feisal Jatnika,Asaki Nagashima,Wakana Miyahara,Abdur Rafique,Yuji Ito
摘要
Antibody delivery across the blood-brain barrier (BBB) remains challenging. We combined phage display with next-generation sequencing (NGS)-guided clone sequence-diverse selection to identify transferrin receptor 1 (TfR1)-binding VHH antibodies. Following alpacas immunization with human and rat TfR1, representative clones from distinct phylogenetic groups were screened for human/mouse cross-reactivity. Three clones (A1, Y11, and Z1) were reformatted as human Fc-mutant fusion proteins and characterized by ELISA, flow cytometry, and fluorescence imaging. All three clones recognized human and mouse TfR1, with ELISA EC₅₀ >100 nM. After intravenous administration in mice, clone Y11 showed sustained brain-associated fluorescence up to 48 h, whereas A1 showed an initially high signal that progressively declined. Fluorescent microscopy revealed preferential localization of Y11 to NeuN-positive neuronal regions, whereas A1 to lectin-positive vascular structures, indicating distinct brain localization profiles among the isolated clones. These findings identify cross-reactive TfR1-targeting VHHs with distinct brain-localization profiles and potential utility as platforms for compartment-selective CNS drug delivery.
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