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

被引:22
|
作者
Yeh, Po-Ying [1 ,2 ]
Chen, Yih-Ruey [1 ]
Wang, Chien-Fang [1 ]
Chang, Ying-Chih [1 ]
机构
[1] Acad Sinica, Genom Res Ctr, 128,Sec 2,Acad Rd, Taipei 115, Taiwan
[2] Stanford Univ, Dept Chem Engn, Stanford, CA 94305 USA
关键词
CIRCULATING TUMOR-CELLS; BREAST-CANCER; ENHANCED CAPTURE; METASTASIS; TECHNOLOGIES; CHALLENGES; GENERATION; BINDING; BLOOD;
D O I
10.1021/acs.biomac.7b01515
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
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页码:426 / 437
页数:12
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