Critical desiccation state Raman spectroscopy for simple, rapid and sensitive detection of native and glycosylated protein. (May 2017)

• Record Type: Journal Article
• Authors: Dai, Qingyuan; Zhu, Xiuling; Yu, Jingyang; Karangwa, Eric; Xia, Shuqin; Zhang, Xiaoming; Jia, Chengsheng
• Is Part Of: Food hydrocolloids. Volume 66(2017)
• Page Start: 90
• Page End: 98
• Publication Date: 2017-05
• Subjects: Raman spectroscopy -- Glycosylated protein -- Zein -- Whey protein isolate -- Dextran; Hydrocolloids -- Periodicals; Food additives -- Periodicals; Colloïdes -- Périodiques; Aliments -- Additifs -- Périodiques; Colloids; Food additives; Periodicals; Electronic journals; 664.06
• DOI: 10.1016/j.foodhyd.2016.12.026
• Languages: English
• ISSNs: 0268-005X

Abstract

Abstract: A simple, rapid, and sensitive method named critical desiccation state Raman spectroscopy (CDSRS) has been developed for detecting native and glycosylated protein. Raman spectroscopy was performed within 1 min and without background subtraction. Results showed that Raman intensity of 1 μL of low concentration dispersions of biomacromolecule analytes remarkably increased from weak to high signal-to-noise ratio during the progressive desiccation process, and high-quality CDSRS spectra of biomacromolecule analytes could easily be obtained under the critical desiccation state, especially those such as zein and whey protein isolate-dextran conjugate which were difficult and even impossible to detect from their solid powders or low concentration dispersions by conventional Raman spectroscopy. Therefore, CDSRS would provide an opportunity to obtain high-quality Raman spectra from biomacromolecule analytes, which would be beneficial to elucidate the relationship between secondary structures and functional properties of protein and to control the formation of food hydrocolloids with desirable physicochemical properties. Graphical abstract: Highlights: A simple, rapid, and sensitive method named critical desiccation state Raman spectroscopy (CDSRS) was developed. CDSRS were performed using 1 μL of low concentration dispersions. CDSRS spectra could be obtained within a minute and without background subtraction. CDSRS spectra of zein and glycosylated protein could easily be obtained.