AI Article Synopsis

  • The study addresses the challenge of isolating cells based on their secreted proteins by using a high-throughput method that integrates heterofunctional particles and fluorescence-activated cell sorting (FACS).
  • The authors successfully isolate antibody-secreting cells (ASCs) that are specific for the H1 protein of the influenza virus from B cells by capturing their secreted immunoglobulins with these particles.
  • The method shows high sensitivity (96%) and specificity (98%) for targeted hybridoma cells, ultimately demonstrating a significant enrichment of H1-specific ASCs through the use of optimized particle designs.

Article Abstract

Isolating cells based on their secreted proteins remain a challenge. The authors demonstrate a capacity for high throughput single-cell protein secretion analysis and isolation based on heterofunctional particles combined with fluorescence activated cell sorting (FACS). The workflow shows that antibody secreting cells (ASCs) specific for the H1 protein from influenza virus can be isolated from B cells. The workflow consists of incubating anti-CD27 particles with the ASCs, capturing locally secreted immunoglobulins with Protein G on the particles, and identifying immunoglobulins specific to H1 via fluorescent labeled antigens followed by FACS to enrich antigen-specific ASCs. Two particles designs, Janus and mixed, are tested with hybridoma cells. Mixed particles are found to improve antibody collection, while Janus particles are found to bind target cells more effectively. Targeted hybridoma cells in coculture with non-specific hybridoma cells are identified with a sensitivity of 96% and specificity of 98%. Heterofunctional particles are used to capture ASCs that secrete antibodies specific for influenza virus from B cells from healthy adults isolated from blood after vaccination. Positive H1-tetramer sorted ASCs are validated using single ASC cultures and identify 23/56 cells specific for H1 demonstrating 164-fold enrichment from total B cells and 14.6-fold enrichment from total ASCs.

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http://dx.doi.org/10.1002/adhm.202001947DOI Listing

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Article Synopsis
  • The study addresses the challenge of isolating cells based on their secreted proteins by using a high-throughput method that integrates heterofunctional particles and fluorescence-activated cell sorting (FACS).
  • The authors successfully isolate antibody-secreting cells (ASCs) that are specific for the H1 protein of the influenza virus from B cells by capturing their secreted immunoglobulins with these particles.
  • The method shows high sensitivity (96%) and specificity (98%) for targeted hybridoma cells, ultimately demonstrating a significant enrichment of H1-specific ASCs through the use of optimized particle designs.
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Lipase from Thermomyces lanuginosus (TLL) was immobilized onto a novel heterofunctional support, divinyl sulfone (DVS) superparamagnetic nanoparticles (SPMNs) functionalized with polyethyleneimine (PEI). Particle size and zeta potential measurements, elemental analysis, X-ray powder diffraction, magnetic measurements, and infrared spectroscopy analysis were used to characterize the TLL preparations. At pH 10, it was possible to achieve 100 % of immobilization yield in 1 h.

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We report the synthesis of a structurally diverse amphiphilic dendrimer with oxidation and ultraviolet light-sensitive groups incorporated in the dendrimer interior. Convergent synthesis is utilized by reacting branched repeating units with a nonbranched functional molecule by two synthetic strategies, Passerini multicomponent reaction and azide-alkyne cycloaddition reaction. The periphery of dendrimer was functionalized by methoxy poly(ethylene glycol) to obtain a dendrimer with a hydrophobic core and hydrophilic peripheral chains.

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