Enhanced Cell Surface Polymer Grafting in Concentrated and Nonreactive Aqueous Polymer Solutions

被引:53
作者
Rossi, Nicholas A. A. [1 ,2 ,3 ]
Constantinescu, Iren [1 ,2 ]
Brooks, Donald E. [1 ,2 ,4 ]
Scott, Mark D. [1 ,2 ,3 ]
Kizhakkedathu, Jayachandran N. [1 ,2 ]
机构
[1] Univ British Columbia, Ctr Blood Res, Vancouver, BC V6T 1Z3, Canada
[2] Univ British Columbia, Dept Pathol & Lab Med, Vancouver, BC V6T 1Z3, Canada
[3] Univ British Columbia, Life Sci Ctr, Canadian Blood Serv, Vancouver, BC V6T 1Z3, Canada
[4] Univ British Columbia, Dept Chem, Vancouver, BC V6T 2B5, Canada
基金
加拿大创新基金会; 加拿大健康研究院;
关键词
RED-BLOOD-CELLS; STEALTH ERYTHROCYTES; VIRAL NANOPARTICLES; DNA DELIVERY; PEGYLATION; DEPLETION; DEXTRAN; CONSEQUENCES; AGGREGATION; CHEMISTRY;
D O I
10.1021/ja909174x
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Macromolecular cell surface modification techniques have shown tremendous utility in various biomedical applications. However, a major drawback concerns inefficient cell surface modification caused by the poor association of hydrophilic macromolecules with cell surfaces. Here, a novel, highly efficient, and universal strategy in which nonreactive "additive" macromolecules are used to modulate the grafting efficiency of cell surface reactive, hydrophilic macromolecules is described. Unprecedented enhanced cell surface modifications by up to 10-fold were observed when various concentrations of a suitable "additive" polymer was present with a constant and low concentration of a "reactive" macromolecule. The importance of this increased efficiency and the possible mechanisms involved are discussed. The cell compatible technique is demonstrated in the case of four different cell types red blood cells (ABC), leukocytes, platelets, and Jurkat cells. A practical application of grafting macromolecules to cell surfaces in concentrated polymer solutions is demonstrated by the enhanced camouflage of ABC surface antigens for the development of RhD null RBC. In principle, the technique can be adapted to various macromolecular systems and cell types, with significant potential for biomedical applications such as live cell based technologies.
引用
收藏
页码:3423 / 3430
页数:8
相关论文
共 34 条
[1]   Biophysical consequences of linker chemistry and polymer size on stealth erythrocytes: size does matter [J].
Bradley, AJ ;
Murad, KL ;
Regan, KL ;
Scott, MD .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 2002, 1561 (02) :147-158
[2]   PEGylation of native disulfide bonds in proteins [J].
Brocchini, Steve ;
Balan, Sibu ;
Godwin, Antony ;
Choi, Ji-Won ;
Zloh, Mire ;
Shaunak, Sunil .
NATURE PROTOCOLS, 2006, 1 (05) :2241-2252
[3]   Comparative analysis of polymer and linker chemistries on the efficacy of immunocamouflage of murine leukocytes [J].
Chen, Audrey M. ;
Scott, Mark D. .
ARTIFICIAL CELLS BLOOD SUBSTITUTES AND BIOTECHNOLOGY, 2006, 34 (03) :305-322
[4]  
Dellacherie E., 1996, POLYSACCHARIDES MED, P525
[5]   Folic acid-mediated targeting of cowpea mosaic virus particles to tumor cells [J].
Destito, Giuseppe ;
Yeh, Robert ;
Rae, Chris S. ;
Finn, M. G. ;
Manchester, Marianne .
CHEMISTRY & BIOLOGY, 2007, 14 (10) :1152-1162
[6]   Structural and biophysical characterization of the 40 kDa PEG-interferon-α2a and its individual positional isomers [J].
Dhalluin, C ;
Ross, A ;
Leuthold, LA ;
Foser, S ;
Gsell, B ;
Müller, F ;
Senn, H .
BIOCONJUGATE CHEMISTRY, 2005, 16 (03) :504-517
[7]   Tissue cells feel and respond to the stiffness of their substrate [J].
Discher, DE ;
Janmey, P ;
Wang, YL .
SCIENCE, 2005, 310 (5751) :1139-1143
[8]   Chemical Modification with High Molecular Weight Polyethylene Glycol Reduces Transduction of Hepatocytes and Increases Efficacy of Intravenously Delivered Oncolytic Adenovirus [J].
Doronin, Konstantin ;
Shashkova, Elena V. ;
May, Shannon M. ;
Hofherr, Sean E. ;
Barry, Michael A. .
HUMAN GENE THERAPY, 2009, 20 (09) :975-988
[9]  
Fleer G.J., 1998, Polymers at Interfaces
[10]  
HSIAO SC, 2008, ANGEW CHEM INT EDIT, V47, P8601