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Jie Xiao

Researcher at Shenzhen University

Publications -  5
Citations -  28

Jie Xiao is an academic researcher from Shenzhen University. The author has contributed to research in topics: Antigen & Isothermal titration calorimetry. The author has an hindex of 3, co-authored 4 publications receiving 27 citations.

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Studies on thermodynamic nature of steroselectivity for ruthenium(II) polypyridyl complex binding to DNA

TL;DR: This new finding may be very helpful to understand the nature of steroselective DNA binding of small chiral molecules, and be useful to the development of DNA molecular probes and new DNA targeting therapeutic drugs.
Journal Article

Studies on thermal denaturation of peanut allergen Ara h1 and its interaction with reducing sugars

TL;DR: The experimental results indicate that the secondary structure of Ara h1 changes significantly along with decreasing alpha-helical structure and its allergenicity with the temperature higher than 85 degrees C, and that both xylose and fructose can stabilize Ara h 1 protein structure through interacting with Ara h2 protein and decrease its allenicity obviously.
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Effect of Electronic Structures of Enantiomers of Ruthenium(II) Polypyridyl Complexes on DNA Binding Behaviors

TL;DR: In this article, a pair of Ru(II) complex enantiomers, Δ- and Λ-[Ru(bpy)2(p-mpip)]2+ {bpy=2,2′-bipyridine, pmpip=2-(4-methylphenyl)imidazo[4,5-f]-1,10-phenanthroline} have been synthesized and structurally characterized.
Journal Article

[Spectroscopic studies on refolding process in vitro of pan-allergen profilin in coco pollen].

TL;DR: Refolding process of recombinant pan-allergen profilin protein induced by urea has been investigated by using circular dichroism spectra, fluorescence spectRA, synchronous fluorescence Spectra systematically, and the spectral characteristics of the renaturation were obtained.
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Hemolytic disease of the newborn due to anti-Jra from a Chinese mother with one novel and one classic heterozygous mutation.

TL;DR: In this paper , the anti-Jra antibody is generated when a Jr(a-) individual pregnant or transfused with Jr (a+) blood unit, which can lead to mild-to-moderate hemolytic disease of the foetus and newborn (HDFN) or hemolysis transfusion reaction (HTR).