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1.
Anal Chem ; 95(33): 12349-12357, 2023 08 22.
Article in English | MEDLINE | ID: mdl-37524054

ABSTRACT

Lipopolysaccharide (LPS) is a bacterial toxin that causes fever in humans. Our small-molecule chemosensor named Zn-dpa-C2OPy shows rapid ratiometric fluorescence response to LPS in water with a detection limit of 11 pM, which is lower than that of our previously reported sensor. Spectroscopic measurements (fluorescence, absorbance, 1H NMR, and fluorescence lifetime), dynamic light scattering measurements, and transmission electron microscopy observations revealed that the fluorescence response was induced by the changes in the aggregation state via multi-point recognition of LPS through hydrophobic and electrostatic interactions, in addition to the coordination between the zinc(II)-dipicolylamine moiety of the chemosensor and the phosphate group of LPS. The proposed Zn-dpa-C2OPy chemosensor was applied to an original flow injection analysis (FIA) system with a self-developed dual-wavelength fluorophotometer, and a high throughput of 36 samples per hour was achieved. These results demonstrate the feasibility of this unique methodology combining a ratiometric fluorescent chemosensor and FIA for continuous online monitoring of LPS in water.


Subject(s)
Lipopolysaccharides , Water , Humans , Water/chemistry , Fluorescent Dyes/chemistry , Zinc/chemistry , Spectrometry, Fluorescence/methods
2.
Cardiol Young ; 19(5): 482-5, 2009 Sep.
Article in English | MEDLINE | ID: mdl-19678963

ABSTRACT

We analysed the GATA binding protein 4 gene, or GATA4, along with the NK2 transcription factor related, locus 5 gene, or NKX2.5, to determine their genetic contribution to 104 sporadic patients in Indonesia with congenitally malformed hearts, 76 cases having atrial septal defect and 28 tetralogy of Fallot. We found only 1 novel mutation of GATA4 in those with atrial septal defects. Analysis of the genetic background of the parents of the patient showed for the first time that a new mutation of GATA4 can cause sporadic atrial septal defects. We failed to discover any other mutations of either the GATA4 or NKX2-5 genes, supporting the marked genetic heterogeneity of human congenital cardiac defects.


Subject(s)
GATA4 Transcription Factor/genetics , Genetic Testing , Heart Septal Defects, Atrial/genetics , Mutation , Tetralogy of Fallot/genetics , Child, Preschool , Humans , Male , Pedigree
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