Scholarlink

<p>Targeting cells for ablation, gene therapy or drug delivery is an ongoing challenge in development of therapeutics. With the goal of efficiently labeling cell surfaces based on target recognition, we linked the well-established engineered ultraID biotin ligase to cell-surface affinity reagents to enable catalytic installation of tags on the surface of cells. Biotin ligase conjugated to nanobodies against cell surface proteins exhibited an order of magnitude increase in cell labeling compared to nanobody alone. Biotin labeling of cells remained efficient at low nanomolar concentrations of the conjugate, and was stable for at least 4&#xa0;h. By testing a swath of antibody-biotin ligase conjugates against various targets and cell types, we confirmed the feasibility and generalizability of this approach. Administration of biotin ligase-conjugated antibodies into animals efficiently biotinylated the expected target cells. Biotinylated target cells were subsequently detectable with fluorescent streptavidin injected into the same mice. Enzyme mediated cell targeting thus provides an efficient and modular platform for biotinylation and detection of cells expressing specific surface targets with potential applications for research and therapeutics.</p>

错误：搜索内容不能为空，请输入英文关键词
错误：关键词超出字数限制，请精简
高级检索

An affinity reagent-conjugated biotin ligase for amplified cell surface labelling in vitro and in vivo

  • 期刊论文

  • 出版模式：

    开放获取

  • 发表日期：

    2026年4月8日

查看全文
  • Beck Holden,
  • Mohammed Mutaher,
  • Raktima Raychowdhury,
  • Matt Bakalar,
  • Abraham Lopez,
  • Marc A. Schwartz,
  • Esther Olajide,
  • Marina Santos,
  • Nir Hacohen

摘要

Targeting cells for ablation, gene therapy or drug delivery is an ongoing challenge in development of therapeutics. With the goal of efficiently labeling cell surfaces based on target recognition, we linked the well-established engineered ultraID biotin ligase to cell-surface affinity reagents to enable catalytic installation of tags on the surface of cells. Biotin ligase conjugated to nanobodies against cell surface proteins exhibited an order of magnitude increase in cell labeling compared to nanobody alone. Biotin labeling of cells remained efficient at low nanomolar concentrations of the conjugate, and was stable for at least 4 h. By testing a swath of antibody-biotin ligase conjugates against various targets and cell types, we confirmed the feasibility and generalizability of this approach. Administration of biotin ligase-conjugated antibodies into animals efficiently biotinylated the expected target cells. Biotinylated target cells were subsequently detectable with fluorescent streptavidin injected into the same mice. Enzyme mediated cell targeting thus provides an efficient and modular platform for biotinylation and detection of cells expressing specific surface targets with potential applications for research and therapeutics.