Abstract：
:In this paper, we describe the preparation and characterization of Langmuir and Langmuir-Blodgett (LB) monolayers of the enzyme organophosphorus acid anhydrolase (OPAA). Langmuir films of OPAA were characterized on different subphases, such as phosphate, ammonium carbonate, and bis-tris-propane buffers. Monolayers at the air-water interface were characterized by measuring the surface pressure and surface potential-area isotherms. In situ UV-vis absorption spectra were also recorded from the Langmuir monolayers. The enzyme activity at the air-water interface was tested by the addition of diisopropylfluorophosphate (DFP) to the subphase. LB films of OPAA were transferred to mica substrates to be studied by atomic force microscopy. Finally, a one-layer LB film of OPAA labeled with a fluorescent probe, fluorescein isothiocyanate (FITC), was deposited onto a quartz slide to be tested as sensor for DFP. The clear, pronounced response and the stability of the LB film as a DFP sensor show the potential of this system as a biosensor.
journal_name
Biomacromoleculesjournal_title
Biomacromoleculesauthors
Mello SV,Mabrouki M,Cao X,Leblanc RM,Cheng TC,DeFrank JJdoi
10.1021/bm025775+keywords:
subject
Has Abstractpub_date
2003-07-01 00:00:00pages
968-73issue
4eissn
1525-7797issn
1526-4602journal_volume
4pub_type
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