TY - JOUR
T1 - Quantitative ligand immobilization using alginate hydrogel formed in a capillary
T2 - Application for online affinity concentration
AU - Fukushima, Yudai
AU - Naito, Toyohiro
AU - Sueyoshi, Kenji
AU - Kubo, Takuya
AU - Kitagawa, Fumihiko
AU - Otsuka, Koji
PY - 2014/6/17
Y1 - 2014/6/17
N2 - To simplify a quantitative immobilization procedure of ligands with maintaining their activities, we developed an automated preparation method using an alginate hydrogel partially formed in a capillary. After a sodium alginate solution containing a ligand was injected into the capillary, a background solution containing Ca2+ was then introduced into the sodium alginate solution zone by applying an appropriate voltage for the hydrogelation, resulting in encapsulation of the ligand by the formed alginate hydrogel. According to the estimated binding capacity for biotin by the encapsulated avidin, the injected avidin was immobilized quantitatively by the formed hydrogel with keeping its affinity. When avidin (3.5-35.2 ng) was immobilized by the proposed method, the immobilization efficiency was estimated to be almost 100%. Furthermore, by using the prepared capillary, biotinylated fluorescein was specifically trapped and separated due to the affinity of the encapsulated avidin. By the change of pH of the background solution, the concentrated analytes could be easily eluted, resulting in 90% recovery with high reproducibility by using 1.18 fmol biotinylated sample.
AB - To simplify a quantitative immobilization procedure of ligands with maintaining their activities, we developed an automated preparation method using an alginate hydrogel partially formed in a capillary. After a sodium alginate solution containing a ligand was injected into the capillary, a background solution containing Ca2+ was then introduced into the sodium alginate solution zone by applying an appropriate voltage for the hydrogelation, resulting in encapsulation of the ligand by the formed alginate hydrogel. According to the estimated binding capacity for biotin by the encapsulated avidin, the injected avidin was immobilized quantitatively by the formed hydrogel with keeping its affinity. When avidin (3.5-35.2 ng) was immobilized by the proposed method, the immobilization efficiency was estimated to be almost 100%. Furthermore, by using the prepared capillary, biotinylated fluorescein was specifically trapped and separated due to the affinity of the encapsulated avidin. By the change of pH of the background solution, the concentrated analytes could be easily eluted, resulting in 90% recovery with high reproducibility by using 1.18 fmol biotinylated sample.
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U2 - 10.1021/ac501039j
DO - 10.1021/ac501039j
M3 - Article
C2 - 24821275
AN - SCOPUS:84902794756
SN - 0003-2700
VL - 86
SP - 5977
EP - 5982
JO - Analytical Chemistry
JF - Analytical Chemistry
IS - 12
ER -