Promoting Multivalent Antibody-Antigen Interactions by Tethering Antibody Molecules on a PEGylated Dendrimer-Supported Lipid Bilayer.
Po-Ying YehYih-Ruey ChenChien-Fang WangYing-Chih ChangPublished in: Biomacromolecules (2018)
To efficiently isolate maximal quantity of circulating tumor cells (CTCs) and circulating tumor cell microembolis (CTMs) from patient blood by antibody coated microfluidics, a multifunctional, pegylated polyamidoamine-dendrimers conjugated supported lipid bilayer surface construct was proposed to enhance accessibility of antibody molecules to the antigen molecules on target CTCs. The combination of a hydrated, stretchable dendrimer and a laterally mobile supported lipid bilayer (SLB) provide attached antibody molecules with 2.5-dimensional chain movement, achieving multivalency between the surface antibody and cell antigen molecules. An over 170% enhancement is distinctive for Panc-1 cells that expresses low antigen level. Of seven pancreatic ductal adenocarcinoma patients, an average 440 single CTCs and 90 CTMs were collected in 2 mL of peripheral blood, which were 1.6 times and 2.3 times more, than those captured by the SLB-only microfluidics. In summary, we have demonstrated a material design to enhance multivalent antibody-antigen interaction, which is useful for rare cell enrichment and cancer detection.
Keyphrases
- circulating tumor cells
- circulating tumor
- single cell
- peripheral blood
- cell therapy
- end stage renal disease
- blood pressure
- drug delivery
- ejection fraction
- chronic kidney disease
- fatty acid
- stem cells
- newly diagnosed
- papillary thyroid
- squamous cell carcinoma
- cell death
- cancer therapy
- peritoneal dialysis
- cell cycle arrest
- label free
- high intensity
- quantum dots