Effect of phospholipid insertion on arrayed polydiacetylene biosensors

Kyung Woo Kim; Hyun Choi; Gil Sun Lee; Dong June Ahn; Min Kyu Oh

doi:10.1016/j.colsurfb.2008.06.020

Effect of phospholipid insertion on arrayed polydiacetylene biosensors

Kyung Woo Kim, Hyun Choi, Gil Sun Lee, Dong June Ahn, Min Kyu Oh

Research output: Contribution to journal › Article › peer-review

48 Citations (Scopus)

Abstract

Micro-arrayed polydiacetylene (PDA) vesicles mixed with phospholipids on glass slides were prepared for label-free detection of Escherichia coli. When E. coli bound to its antibodies chemically attached to polydiacetylene, the fluorescence of the vesicles was dramatically increased. The insertion of dimyristoyl phosphatidylcholine (DMPC) in the vesicles drastically reduced the response time for the fluorescence changes. Vesicles with 20-30% DMPC provided optimal results for bacterial detection. Fourier transform infrared (FTIR) spectra analysis suggested that DMPC insertion decreased the strength of hydrogen bonding among the amide and carboxylic acid groups of the polydiacetylene vesicles. Reduced bonding strength resulted in less rigid structure of the polydiacetylene polymer, allowing more rapid detection upon molecular recognition.

Original language	English
Pages (from-to)	213-217
Number of pages	5
Journal	Colloids and Surfaces B: Biointerfaces
Volume	66
Issue number	2
DOIs	https://doi.org/10.1016/j.colsurfb.2008.06.020
Publication status	Published - 2008 Oct 15

Keywords

Bacteria sensor
Dimyristoyl phosphatidylcholine (DMPC)
FTIR
Label-free biosensor
Polydiacetylene

ASJC Scopus subject areas

Biotechnology
Surfaces and Interfaces
Physical and Theoretical Chemistry
Colloid and Surface Chemistry

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10.1016/j.colsurfb.2008.06.020

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title = "Effect of phospholipid insertion on arrayed polydiacetylene biosensors",

abstract = "Micro-arrayed polydiacetylene (PDA) vesicles mixed with phospholipids on glass slides were prepared for label-free detection of Escherichia coli. When E. coli bound to its antibodies chemically attached to polydiacetylene, the fluorescence of the vesicles was dramatically increased. The insertion of dimyristoyl phosphatidylcholine (DMPC) in the vesicles drastically reduced the response time for the fluorescence changes. Vesicles with 20-30% DMPC provided optimal results for bacterial detection. Fourier transform infrared (FTIR) spectra analysis suggested that DMPC insertion decreased the strength of hydrogen bonding among the amide and carboxylic acid groups of the polydiacetylene vesicles. Reduced bonding strength resulted in less rigid structure of the polydiacetylene polymer, allowing more rapid detection upon molecular recognition.",

keywords = "Bacteria sensor, Dimyristoyl phosphatidylcholine (DMPC), FTIR, Label-free biosensor, Polydiacetylene",

author = "Kim, {Kyung Woo} and Hyun Choi and Lee, {Gil Sun} and Ahn, {Dong June} and Oh, {Min Kyu}",

note = "Funding Information: This research was supported partly by the Korea Research Foundation (KRF-2006-005-J03603), the Ministry of Health and Welfare (MOH-A050750), Korea Science and Engineering Foundation (Protein Chip Technology program), the Korea Foundation for International Cooperation of Science & Technology, and the Brain Korea 21 Project.",

year = "2008",

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doi = "10.1016/j.colsurfb.2008.06.020",

language = "English",

volume = "66",

pages = "213--217",

journal = "Colloids and Surfaces B: Biointerfaces",

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AU - Kim, Kyung Woo

AU - Choi, Hyun

AU - Lee, Gil Sun

AU - Ahn, Dong June

AU - Oh, Min Kyu

N1 - Funding Information: This research was supported partly by the Korea Research Foundation (KRF-2006-005-J03603), the Ministry of Health and Welfare (MOH-A050750), Korea Science and Engineering Foundation (Protein Chip Technology program), the Korea Foundation for International Cooperation of Science & Technology, and the Brain Korea 21 Project.

PY - 2008/10/15

Y1 - 2008/10/15

N2 - Micro-arrayed polydiacetylene (PDA) vesicles mixed with phospholipids on glass slides were prepared for label-free detection of Escherichia coli. When E. coli bound to its antibodies chemically attached to polydiacetylene, the fluorescence of the vesicles was dramatically increased. The insertion of dimyristoyl phosphatidylcholine (DMPC) in the vesicles drastically reduced the response time for the fluorescence changes. Vesicles with 20-30% DMPC provided optimal results for bacterial detection. Fourier transform infrared (FTIR) spectra analysis suggested that DMPC insertion decreased the strength of hydrogen bonding among the amide and carboxylic acid groups of the polydiacetylene vesicles. Reduced bonding strength resulted in less rigid structure of the polydiacetylene polymer, allowing more rapid detection upon molecular recognition.

AB - Micro-arrayed polydiacetylene (PDA) vesicles mixed with phospholipids on glass slides were prepared for label-free detection of Escherichia coli. When E. coli bound to its antibodies chemically attached to polydiacetylene, the fluorescence of the vesicles was dramatically increased. The insertion of dimyristoyl phosphatidylcholine (DMPC) in the vesicles drastically reduced the response time for the fluorescence changes. Vesicles with 20-30% DMPC provided optimal results for bacterial detection. Fourier transform infrared (FTIR) spectra analysis suggested that DMPC insertion decreased the strength of hydrogen bonding among the amide and carboxylic acid groups of the polydiacetylene vesicles. Reduced bonding strength resulted in less rigid structure of the polydiacetylene polymer, allowing more rapid detection upon molecular recognition.

KW - Bacteria sensor

KW - Dimyristoyl phosphatidylcholine (DMPC)

KW - FTIR

KW - Label-free biosensor

KW - Polydiacetylene

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U2 - 10.1016/j.colsurfb.2008.06.020

DO - 10.1016/j.colsurfb.2008.06.020

M3 - Article

C2 - 18701264

AN - SCOPUS:50649088906

VL - 66

SP - 213

EP - 217

JO - Colloids and Surfaces B: Biointerfaces

JF - Colloids and Surfaces B: Biointerfaces

SN - 0927-7765

IS - 2

ER -

Effect of phospholipid insertion on arrayed polydiacetylene biosensors

Abstract

Keywords

ASJC Scopus subject areas

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