TY - JOUR
T1 - Enhancement of enzymatic colorimetric response by silver island films on high throughput screening microplates
AU - Abel, Biebele
AU - Clement, Travis C.
AU - Aslan, Kadir
N1 - Publisher Copyright:
© 2014 Elsevier B.V.
PY - 2014/9/1
Y1 - 2014/9/1
N2 - In this study, we report the use of an enzyme-based hybrid platform, which is comprised of silver island films, enzymes (HRP and AP) and high-throughput screening (HTS) microplates, to enhance the colorimetric response of enzymatic reactions. The hybrid platform was designed in a two-step process: (i) deposition of SIFs onto HTS microplates with low, medium, and high loading (refers to the extent of the surface plasmon resonance peak of SIFs at 460. nm) using Tollen's reaction scheme; and (ii) attachment of b-BSA or BEA as linkers for the immobilization of enzymes. The presence of SIFs within the wells of the HTS microplates was confirmed using an optical spectrophotometer and real-color photography. Control experiments, where SIFs were omitted from the surfaces were carried out to confirm the effect of SIFs on the enzymatic colorimetric response. Significant colorimetric signal enhancement was observed for HRP or AP on SIFs (high loading) deposited HTS microplates using b-BSA (up to ~ 3-fold for AP and ~ 6-fold HRP) or BEA (up to ~ 7-fold for both HRP and AP), as compared to our control samples. The observed increase in colorimetric response can be attributed to the nature of BEA, which exposes surface-bound enzymes to the substrate present in bulk more efficiently than b-BSA. This study proves that SIFs can serve as a valuable tool to improve the signal output of existing bioassays carried out in HTS microplates, which can be applicable to the field biosensors and plasmonics.
AB - In this study, we report the use of an enzyme-based hybrid platform, which is comprised of silver island films, enzymes (HRP and AP) and high-throughput screening (HTS) microplates, to enhance the colorimetric response of enzymatic reactions. The hybrid platform was designed in a two-step process: (i) deposition of SIFs onto HTS microplates with low, medium, and high loading (refers to the extent of the surface plasmon resonance peak of SIFs at 460. nm) using Tollen's reaction scheme; and (ii) attachment of b-BSA or BEA as linkers for the immobilization of enzymes. The presence of SIFs within the wells of the HTS microplates was confirmed using an optical spectrophotometer and real-color photography. Control experiments, where SIFs were omitted from the surfaces were carried out to confirm the effect of SIFs on the enzymatic colorimetric response. Significant colorimetric signal enhancement was observed for HRP or AP on SIFs (high loading) deposited HTS microplates using b-BSA (up to ~ 3-fold for AP and ~ 6-fold HRP) or BEA (up to ~ 7-fold for both HRP and AP), as compared to our control samples. The observed increase in colorimetric response can be attributed to the nature of BEA, which exposes surface-bound enzymes to the substrate present in bulk more efficiently than b-BSA. This study proves that SIFs can serve as a valuable tool to improve the signal output of existing bioassays carried out in HTS microplates, which can be applicable to the field biosensors and plasmonics.
KW - Alkaline phosphatase
KW - Biotin-poly(ethylene-glycol)amine
KW - High-throughput screening microplates
KW - Horseradish peroxidase
KW - Plasmonic nanoparticles
KW - Silver island films
UR - http://www.scopus.com/inward/record.url?scp=84907090931&partnerID=8YFLogxK
U2 - 10.1016/j.jim.2014.06.005
DO - 10.1016/j.jim.2014.06.005
M3 - Article
C2 - 24950456
AN - SCOPUS:84907090931
SN - 0022-1759
VL - 411
SP - 43
EP - 49
JO - Journal of Immunological Methods
JF - Journal of Immunological Methods
ER -