TY - JOUR
T1 - Development of Enzyme Loaded Polyion Complex Vesicle (PICsome)
T2 - Thermal Stability of Enzyme in PICsome Compartment and Effect of Coencapsulation of Dextran on Enzyme Activity
AU - Tang, Hengmin
AU - Sakamura, Yuki
AU - Mori, Takeshi
AU - Katayama, Yoshiki
AU - Kishimura, Akihiro
N1 - Funding Information:
This research was financially supported in part by a Grant-in-Aid for Scientific Research (Grant No. 26288082) from the Ministry of Education, Culture, Sports, Science, and Technology (MEXT) of Japan and the Mochida Memorial Foundation for Medical and Pharmaceutical Research. The authors are grateful to the Nanotechnology Platform Project (Molecules and Materials Synthesis) of the MEXT. The authors are grateful to Prof. M. Murata and Dr. T. Kawano (Center for Advanced Medical Innovation, Kyushu University) for their technical support of FCS measurements.
Publisher Copyright:
© 2017 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
PY - 2017/8
Y1 - 2017/8
N2 - Applications of enzymes are intensively studied, particularly for biomedical applications. However, encapsulation or immobilization of enzymes without deactivation and long-term use of enzymes are still at issue. This study focuses on the polymeric vesicles “PICsomes” for encapsulation of enzymes to develop a hecto-nanometer-scaled enzyme-loaded reactor. The catalytic activity of a PICsome-based enzyme nanoreactor is carefully examined to clarify the effect of compartmentalization by PICsome. Encapsulation by PICsome provides a stability enhancement of enzymes after 24 h incubation at 37 °C, which is particularly helpful for maintaining the high effective concentration of β-galactosidase. Moreover, to control the microenvironment inside the nanoreactor, a large amount of dextran, a neutral macromolecule, is encapsulated together with β-galactosidase in the PICsome. The resulting dextran-coloaded nanoreactor contributes to the enhancement of enzyme stability, even after exposure to 24 h incubation at −20 °C, mainly due to the antifreezing effect. (Figure presented.).
AB - Applications of enzymes are intensively studied, particularly for biomedical applications. However, encapsulation or immobilization of enzymes without deactivation and long-term use of enzymes are still at issue. This study focuses on the polymeric vesicles “PICsomes” for encapsulation of enzymes to develop a hecto-nanometer-scaled enzyme-loaded reactor. The catalytic activity of a PICsome-based enzyme nanoreactor is carefully examined to clarify the effect of compartmentalization by PICsome. Encapsulation by PICsome provides a stability enhancement of enzymes after 24 h incubation at 37 °C, which is particularly helpful for maintaining the high effective concentration of β-galactosidase. Moreover, to control the microenvironment inside the nanoreactor, a large amount of dextran, a neutral macromolecule, is encapsulated together with β-galactosidase in the PICsome. The resulting dextran-coloaded nanoreactor contributes to the enhancement of enzyme stability, even after exposure to 24 h incubation at −20 °C, mainly due to the antifreezing effect. (Figure presented.).
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U2 - 10.1002/mabi.201600542
DO - 10.1002/mabi.201600542
M3 - Article
C2 - 28524263
AN - SCOPUS:85019367996
SN - 1616-5187
VL - 17
JO - Macromolecular Bioscience
JF - Macromolecular Bioscience
IS - 8
M1 - 1600542
ER -