TY - JOUR
T1 - Physisorption and chemisorption of T4 bacteriophages on amino functionalized silica particles
AU - Bone, Stephanie
AU - Alum, Absar
AU - Markovski, Jasmina
AU - Hristovski, Kiril
AU - Bar-Zeev, Edo
AU - Kaufman, Yair
AU - Abbaszadegan, Morteza
AU - Perreault, Francois
N1 - Funding Information:
This work was supported by the ASU-BGU Roskind Program for Collaboration through the ASU Foundation and the NSF Nanosystems Engineering Research Center for Nanotechnology-Enabled Water Treatment ( EEC-1449500 ). In addition, it was supported in part by the NSF Water and Environmental Technology Center at ASU. The authors gratefully acknowledge the use of the characterization facilities within the LeRoy Eyring Center for Solid State Science at Arizona State University, as well as Dr. David Lowry and the Electron Microscopy division of the CLAS Bioimaging Facility at ASU. We also thank Ana Barrios for the microscopy images.
Publisher Copyright:
© 2018 Elsevier Inc.
PY - 2018/12/15
Y1 - 2018/12/15
N2 - Bacteriophages, or phages, are receiving increasing interest as recognition tools for the design of bioactive surfaces. However, to maintain the activity of surface-bound phages, the immobilization strategy must provide the right orientation and not compromise the phages’ integrity. The objectives of this study were to characterize the phage sorption capacity and the immobilized phage activity for aminated silica particles functionalized with T4 phages. Two functionalization strategies were compared; physisorption, based on electrostatic adhesion, and chemisorption, where the phage and the particle are coupled using a carbodiimide cross-linker. We report that chemisorption, at maximum adsorption conditions on 1 µm particles, yielded 16 functional phages per particle, which is 2.5 times more than by the physisorption method. Particle diameter is shown to have an important impact on phage attachment and 1.8 µm particles were found to have ∼4 times more phages per surface area than 0.5 µm particles. Higher surface coverage is attributed to the lower steric hindrance on bigger particles. These findings provide important guidelines for the design of phage-functionalized particles for environmental, biomedical, or sensing applications.
AB - Bacteriophages, or phages, are receiving increasing interest as recognition tools for the design of bioactive surfaces. However, to maintain the activity of surface-bound phages, the immobilization strategy must provide the right orientation and not compromise the phages’ integrity. The objectives of this study were to characterize the phage sorption capacity and the immobilized phage activity for aminated silica particles functionalized with T4 phages. Two functionalization strategies were compared; physisorption, based on electrostatic adhesion, and chemisorption, where the phage and the particle are coupled using a carbodiimide cross-linker. We report that chemisorption, at maximum adsorption conditions on 1 µm particles, yielded 16 functional phages per particle, which is 2.5 times more than by the physisorption method. Particle diameter is shown to have an important impact on phage attachment and 1.8 µm particles were found to have ∼4 times more phages per surface area than 0.5 µm particles. Higher surface coverage is attributed to the lower steric hindrance on bigger particles. These findings provide important guidelines for the design of phage-functionalized particles for environmental, biomedical, or sensing applications.
KW - Chemisorption
KW - Phage
KW - Physisorption
KW - Silica particles
KW - T4
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U2 - 10.1016/j.jcis.2018.07.107
DO - 10.1016/j.jcis.2018.07.107
M3 - Article
C2 - 30077067
AN - SCOPUS:85050790993
SN - 0021-9797
VL - 532
SP - 68
EP - 76
JO - Journal of Colloid And Interface Science
JF - Journal of Colloid And Interface Science
ER -