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May 13-14, 2019 | Prague, Czech Republic

Chemistry and Medicinal Chemistry

9

th

World Congress on

Page 50

Asian Journal of Biomedical and Pharmaceutical Sciences | Volume 9

ISSN: 2249-622X

Yaw-Kuen Li

NCTU, Taiwan

Strategy for constructing antifouling biosensors

B

iosensors commonly suffer from seriously non-specific

protein adsorption while measuring real samples

in human serum and consequently lead to unreliable

responses. To improve the accuracy of detection, biosensor

modified with an antifouling surface is indispensable.

Though many strategies for reducing non-specific

interaction have been developed, the task has not been

solved with an acceptable outcome. In particular, after

installing the biorecognizers, such as antibodies, for specific

targets, the anti-fouling feature of a biosensor is commonly

destroyed. How to overcome this problem becomes a

main issue of biosensing. We propose and demonstrate

an effective protocol via electrodeposition of charged-

aniline derivatives for the fabrication of biosensors with

promising antifouling ability. The antifouling layer, denoted

as (N+S) layer, was constructed on various electrodes via

electrodeposition by using the mixture (1:1 molar ratio) of

two opposite charged-aniline derivatives, 4-amino-N, N,

N-trimethylanilinium (N) and 4-aminobenzenesulfonate

(S). In order to know the power of antifouling of (N+S)

surface, we compared its cyclic voltammetric property

and the feature of human serum adhesion with the

common antifouling surfaces (zwitterionic layers and poly

ethylene glycol layers). All the tested surfaces gave similar

antifouling power. Yet, the (N+S)-modified surface showed

excellent conductivity. The antifouling efficiency of the

(N+S) surface is greatly improved with the addition of 1 %

sarcosine in human serum as compared with other tested

surfaces. On top of the “charged layer”, isothiocyanate

moieties can be added on with the desired density

with which scFvs in the form of proteins or, even better,

peptides will be immobilized on the surface of sensor. The

standard protocols of screening with phage display library

or ribosome display library will be briefly discussed.

Speaker Biography

Yaw-Kuen Li received his PhD degree from Tulane University, USA, in

1991. After his postdoctoral research in School of Medicine of Johns

Hopkins University, he moved back to Taiwan to start his academic

career in 1993. He was promoted to a full professor in 2002. Further,

he became the chair of the department in 2004 and the Dean of

college of science in 2014. His primary research interests include

three major fields: (a) Enzyme-based catalytic biological reactions, (b)

Bio-recognition and Bio-sensors, (c) Solid-state/biological interface

chemistry.

e:

nctuykl@g2.nctu.edu.tw

Yaw-Kuen Li, Asian J Biomed Pharmaceut Sci, Volume:9

DOI: 10.4066/2249-622X-C2-019

Notes: