1. Academic Validation
  2. Promoting Multivalent Antibody-Antigen Interactions by Tethering Antibody Molecules on a PEGylated Dendrimer-Supported Lipid Bilayer

Promoting Multivalent Antibody-Antigen Interactions by Tethering Antibody Molecules on a PEGylated Dendrimer-Supported Lipid Bilayer

  • Biomacromolecules. 2018 Feb 12;19(2):426-437. doi: 10.1021/acs.biomac.7b01515.
Po-Ying Yeh 1 2 Yih-Ruey Chen 1 Chien-Fang Wang 1 Ying-Chih Chang 1
Affiliations

Affiliations

  • 1 Genomics Research Center, Academia Sinica , 128, Sec 2, Academic Road, Nankang, Taipei 115, Taiwan.
  • 2 Department of Chemical Engineering, Stanford University , Stanford, California 94305, United States.
Abstract

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.

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