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IMPROVEMENTS IN PROCEDURES FOR PER-O-METHYLATION OF CARBOHYDRATES

IMPROVEMENTS IN PROCEDURES FOR PER-O-METHYLATION OF CARBOHYDRATES
碳水化合物全邻甲基化程序的改进
批准号:
8170854
负责人:
Catherine E. Costello
金额:
$0.69万
依托单位国家:
美国
项目类别:
财政年份:
2010
资助国家:
美国
项目状态:
已结题
起止时间:
2010-06-01 至 2011-05-31

项目摘要

项目成果

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中文摘要
翻译
这个子项目是众多研究子项目之一
英文摘要
This subproject is one of many research subprojects utilizing the resources provided by a Center grant funded by NIH/NCRR. The subproject and investigator (PI) may have received primary funding from another NIH source, and thus could be represented in other CRISP entries. The institution listed is for the Center, which is not necessarily the institution for the investigator. Improved procedures for per-O-methylation of carbohydrates are being developed, based on investigation of the possible oxidative degradation mechanisms occurring during the derivatization in dimethyl sulfoxide with methyl iodide in the presence of base. We have demonstrated that degradation occurs only under anhydrous conditions when there is a long reaction time between the carbohydrate dissolved in dimethyl sulfoxide and methyl iodide, followed by reaction with the base. Evidence was obtained that the degradation occurs only under anhydrous conditions when there is a long reaction time between the carbohydrate dissolved in dimethyl sulfoxide and methyl iodide, followed by reaction with the base. We found that it can be totally avoided by treating the carbohydrate with powdered sodium hydroxide before introduction of methyl iodide under non-anhydrous conditions, or by adding a trace of water in dimethyl sulfoxide before methyl iodide, or by using N, N-dimethyl acetamide as the solvent (Ciucanu and Costello, J. Am. Chem. Soc. , 2003, 125, 16213-16219). Later results reported by others (Novotnoy et al., ASMS 2005) that took advantage of this chemical insight have demonstrated that microscale reactions are feasible using capillaries packed with solid NaOH. We have evaluated this approach, and other steps that may help to improve efficiency and minimizxe contamination for low amounts of sample. We also participated in a round-robin analysis of a set of O-linked glycopeptide samples that were analyzed by several laboratories within a project sponsored by the Human Glycoproteomics Initiative, based in Osaka, Japan. A manuscript describing this was recently published in Molecular and Cellular Proteomics.
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Legacy Support During Closure of the Mass Spectrometry Resource for Biology and Medicine
  • 批准号:
    10204050
  • 项目类别:
  • 资助金额:
    $53.99万
  • 财政年份:
    2019
  • 负责人:
    Catherine E. Costello
  • 依托单位:
Legacy Support During Closure of the Mass Spectrometry Resource for Biology and Medicine
  • 批准号:
    9976561
  • 项目类别:
  • 资助金额:
    $70.81万
  • 财政年份:
    2019
  • 负责人:
    Catherine E. Costello
  • 依托单位:
Legacy Support During Closure of the Mass Spectrometry Resource for Biology and Medicine
  • 批准号:
    9810729
  • 项目类别:
  • 资助金额:
    $82.73万
  • 财政年份:
    2019
  • 负责人:
    Catherine E. Costello
  • 依托单位:
MALDI-TOF/TOF MS TO SUPPORT BIOMEDICAL RESEARCH
  • 批准号:
    8247392
  • 项目类别:
  • 资助金额:
    $59.0万
  • 财政年份:
    2012
  • 负责人:
    Catherine E. Costello
  • 依托单位:
海外基金