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Generation and Screening of Antigen-Specific Nanobodies from Mammalian Cells Expressing the BCR Repertoire Library Using Droplet-Based Microfluidics.
Lyu, Menghua; Shi, Xuyang; Liu, Xiaopan; Liu, Yang; Zhu, Xijun; Liao, Lijuan; Zhao, Hongyan; Sun, Na; Wang, Shiyu; Chen, Linzhe; Fan, Linyuan; Xu, Qumiao; Zhu, Qianqian; Gao, Kai; Chen, Huaying; Zhu, Yonggang; Li, Zida; Guo, Weijin; Zheng, Yue; Gu, Ying; Liu, Longqi; Wang, Meiniang; Liu, Ya.
Afiliación
  • Lyu M; BGI-Shenzhen, Shenzhen 518083, China.
  • Shi X; College of Life Sciences, University of Chinese Academy of Sciences, Beijing 100049, China.
  • Liu X; BGI-Shenzhen, Shenzhen 518083, China.
  • Liu Y; College of Life Sciences, University of Chinese Academy of Sciences, Beijing 100049, China.
  • Zhu X; BGI-Shenzhen, Shenzhen 518083, China.
  • Liao L; BGI-Shenzhen, Shenzhen 518083, China.
  • Zhao H; BGI-Shenzhen, Shenzhen 518083, China.
  • Sun N; BGI-Shenzhen, Shenzhen 518083, China.
  • Wang S; BGI-Shenzhen, Shenzhen 518083, China.
  • Chen L; BGI-Shenzhen, Shenzhen 518083, China.
  • Fan L; BGI-Shenzhen, Shenzhen 518083, China.
  • Xu Q; Department of Biomedical Engineering, School of Medicine, Shenzhen University, Shenzhen 518060, China.
  • Zhu Q; BGI-Shenzhen, Shenzhen 518083, China.
  • Gao K; College of Life Sciences, University of Chinese Academy of Sciences, Beijing 100049, China.
  • Chen H; BGI-Shenzhen, Shenzhen 518083, China.
  • Zhu Y; BGI-Shenzhen, Shenzhen 518083, China.
  • Li Z; BGI-Shenzhen, Shenzhen 518083, China.
  • Guo W; School of Mechanical Engineering and Automation, Harbin Institute of Technology, Shenzhen, Shenzhen 518055, China.
  • Zheng Y; School of Mechanical Engineering and Automation, Harbin Institute of Technology, Shenzhen, Shenzhen 518055, China.
  • Gu Y; Department of Biomedical Engineering, School of Medicine, Shenzhen University, Shenzhen 518060, China.
  • Liu L; Department of Biomedical Engineering, Shantou University, Shantou 515063, China.
  • Wang M; BGI-Shenzhen, Shenzhen 518083, China.
  • Liu Y; BGI-Shenzhen, Shenzhen 518083, China.
Anal Chem ; 94(22): 7970-7980, 2022 06 07.
Article en En | MEDLINE | ID: mdl-35604850
ABSTRACT
Nanobodies, also known as VHHs, originate from the serum of Camelidae. Nanobodies have considerable advantages over conventional antibodies, including smaller size, more modifiable, and deeper tissue penetration, making them promising tools for immunotherapy and antibody-drug development. A high-throughput nanobody screening platform is critical to the rapid development of nanobodies. To date, droplet-based microfluidic systems have exhibited improved performance compared to the traditional phage display technology in terms of time and throughput. In realistic situations, however, it is difficult to directly apply the technology to the screening of nanobodies. Requirements of plasma cell enrichment and high cell viability, as well as a lack of related commercial reagents, are leading causes for impeding the development of novel methods. We overcame these obstacles by constructing a eukaryotic display system that secretes nanobodies utilizing homologous recombination and eukaryotic transformation technologies, and the significant advantages are that it is independent of primary cell viability and it does not require plasma cell enrichment in advance. Next, a signal capture system of "SA-beads + Biotin-antigen + nanobody-6 × His + fluorescence-labeled anti-6 × His (secondary antibody)" was designed for precise localization of the eukaryotic-expressed nanobodies in a droplet. Based on this innovation, we screened 293T cells expressing anti-PD-L1 nanobodies with a high positive rate of targeted cells (up to 99.8%). Then, single-cell transcriptomic profiling uncovered the intercellular heterogeneity and BCR sequence of target cells at a single-cell level. The complete complementarity determining region (CDR3) structure was obtained, which was totally consistent with the BCR reference. This study expanded the linkage between microfluidic technology and nanobody applications and also showed potential to accelerate the rapid transformation of nanobodies in the large-scale market.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Anticuerpos de Dominio Único Tipo de estudio: Diagnostic_studies / Screening_studies Límite: Animals Idioma: En Revista: Anal Chem Año: 2022 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Anticuerpos de Dominio Único Tipo de estudio: Diagnostic_studies / Screening_studies Límite: Animals Idioma: En Revista: Anal Chem Año: 2022 Tipo del documento: Article País de afiliación: China