Shaoxiang Xiong

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Name: 熊少祥; ShaoXiang Xiong
Organization: Institute of Chemistry, Chinese Academy of Sciences , China
Department:
Title: Researcher/Professor(PhD)

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Co-reporter:Shu Zhang, Jian'an Liu, Yi Chen, Shaoxiang Xiong, Guanghui Wang, Jun Chen, Guoqiang Yang
Journal of the American Society for Mass Spectrometry 2010 Volume 21(Issue 1) pp:154-160
Publication Date(Web):January 2010
DOI:10.1016/j.jasms.2009.09.024
Matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS) does not work efficiently on small molecules (usually with molecular weight below 500 Da) because of the interference of matrix-related peaks in low m/z region. The previous methods developed for this problem focused on reducing the peaks caused by the traditional matrices. Here, we report a novel strategy to analyze small molecules in a high and interference-free mass range by using metal-phthalocyanines (MPcs) as matrices which should be capable of forming matrix-analyte adducts. The mass of the target analyte was calculated by subtracting the mass of MPc from the mass of the MPc–analyte adduct. MPcs were also detectable and could serve as internal standards. Various MPcs with aromatic or aliphatic groups and different metal centers were then synthesized and explored. Aluminum-phthalocyanines (AlPcs), gallium-phthalocyanines (GaPcs), and indium-phthalocyanines (InPcs) were efficient matrices to form MPc–analyte adducts in either the positive or negative ion mode. The detection limits varied from 17 to 75 fmol, depending on analyte types. The mechanism of adducts formation was also proposed. Collectively, our strategy provides a novel and efficient way to analyze small molecules by MALDI-TOF MS.Using metal-phthalocyanines (MPcs) as matrices, small molecules were detected in the form of MPc–analyte adduct in a higher mass region by MALDI-TOF MS.Figure optionsDownload full-size imageDownload high-quality image (52 K)Download as PowerPoint slide
Co-reporter:Shu Zhang, Yi Chen, Jian An Liu, Shao Xiang Xiong, Guang Hui Wang, Jun Chen, Guo Qiang Yang
Chinese Chemical Letters 2009 20(12) pp: 1495-1497
Publication Date(Web):
DOI:10.1016/j.cclet.2009.06.031
L-Arginine, L-α-aspartyl-O-phosphono-L-serylglycyl-L-α-glutamylglycyl-L-α-aspartyl-L-phenylalanyl-L-leucyl-L-alanyl-L-α-glutamylglycylglycylglycyl-L-valyl-
1-Palmitoyl-2-arachidoyllecithin