Abiotic Stimuli-Responsive Protein Affinity Reagent for IgG

被引:12
作者
Onogi, Shunsuke [1 ,2 ]
Lee, Shih-Hui [1 ]
Fruehauf, Krista R. [1 ]
Shea, Kenneth J. [1 ]
机构
[1] Univ Calif Irvine, Dept Chem, Irvine, CA 92697 USA
[2] JSR Corp, Tsukuba Res Labs, Tsukuba, Ibaraki 3050841, Japan
基金
美国国家科学基金会;
关键词
SYNTHETIC-POLYMER NANOPARTICLE; IMMUNOGLOBULIN-G; N-ISOPROPYLACRYLAMIDE; RATIONAL DESIGN; IONIC-STRENGTH; PEPTIDE LIGAND; BINDING; PURIFICATION; PH; HYDROGELS;
D O I
10.1021/acs.biomac.1c00335
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
We describe an approach for the discovery of protein affinity reagents (PARS). Abiotic synthetic hydrogel copolymers can be "tuned" for selective protein capture by the type and ratios of functional monomers included in their polymerization and by the polymerization conditions (i.e., pH). By screening libraries of hydrogel nanoparticles (NPs) containing charged and hydrophobic groups against a protein target (IgG), a stimuli-responsive PAR is selected. The robust carbon backbone synthetic copolymer is rapidly synthesized in the chemistry laboratory from readily available monomers. The production of the PAR does not require living cells and is free from biological contamination. The capture and release of the protein by the copolymer NP is reversible. IgG is sequestered from human serum at pH 6.5 and following a wash step, the purified protein is released by elevating the pH to 7.3. The binding and release of the protein occur without denaturation. The abiotic material functions as a selective PAR for the F(ab')(2) domain of IgG for pull-down and immunoprecipitation experiments and for isolation and purification of proteins from complex biological mixtures.
引用
收藏
页码:2641 / 2648
页数:8
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