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DESCRIPTION (provided by applicant): Currently, the fastest growing areas of high performance liquid chromatographic separations are in the areas of biomolecule separations and liquid chromatography-mass spectrometry (LC-MS). While the last few decades have seen phenomenal progress in mass spectrometry, the shortfalls inherent in the separations coupled to the mass spectrometer still present considerable barriers to accessing the full information content in biological samples. Biomolecule separations are challenging because they present a variety of interaction modalities ranging from hydrophobic to polar to electrostatic. The proposed work addresses the urgent need for improved technologies for novel and more universal separation strategies for biopolymers (e.g., polypeptides, proteins, oligonucleotides) while simultaneously enabling characterization of solute/ionic liquid interactions. The objective of the proposed work is to integrate the emerging field of ionic liquids into novel separation strategies for biomolecular separations with the goal of providing a rapid method for assessing ionic liquids/target analyte interactions a new class of stationary phases enabling separations of complex biomolecular mixtures. We hypothesize that the proposed selectors will provide multimodal retention for the separation of a wide variety of biomolecular analytes. Two specific aims will address this hypothesis: 1. CE Studies of Ionic Liquid Selectors. Capillary electrophoresis will be used to rapidly screen for ionic liquids/selected analyte interactions. We will relate migration data to ionic liquid/analyte affinity. 2. LC Studies of Ionic Liquid Selectors. Retention data will be obtained on the proposed HPLC sorbents beginning systematically with small molecules (e.g., aromatics, nucleotides, amino acids) and extending to larger molecules (e.g., peptides, polynucleotides) as the separation space encompassed by this new media is mapped out.
期刊论文(7)
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DOI: 10.1016/j.chroma.2008.02.048
发表时间: 2008-05
期刊: Journal of chromatography. A
影响因子: --
作者: [D. S. Meter;O. D. Stuart;A. B. Carle;A. Stalcup]
通讯作者: D. S. Meter;O. D. Stuart;A. B. Carle;A. Stalcup
DOI: 10.1016/j.chroma.2010.11.058
发表时间: 2011-01-21
期刊: Journal of chromatography. A
影响因子: --
作者: [Fields PR, Sun Y, Stalcup AM]
通讯作者: Stalcup AM
Heparin-induced circular dichroism of chloroquine.
肝素诱导的氯喹圆二色性。
DOI: 10.1016/j.bbrc.2009.07.098
发表时间: 2009
期刊: Biochemical and biophysical research communications
影响因子: 3.1
作者: [Stanley,FE, Warner,AM, Gutierrez,SM, Stalcup,AM]
通讯作者: Stalcup,AM
Rapid determination of surfactant critical micelle concentrations using pressure-driven flow with capillary electrophoresis instrumentation.
使用毛细管电泳仪器的压力驱动流快速测定表面活性剂临界胶束浓度。
DOI: 10.1016/j.chroma.2009.09.026
发表时间: 2009
期刊: Journal of chromatography. A
影响因子: --
作者: [Stanley,FE, Warner,AM, Schneiderman,E, Stalcup,AM]
通讯作者: Stalcup,AM
Novel Multimodal Selectors for CE and HPLC
  • 批准号:
    7025695
  • 项目类别:
  • 资助金额:
    $20.78万
  • 财政年份:
    2005
  • 负责人:
    Apryll M Stalcup
  • 依托单位:
Novel Multimodal Selectors for CE and HPLC
  • 批准号:
    6901567
  • 项目类别:
  • 资助金额:
    $35.76万
  • 财政年份:
    2005
  • 负责人:
    Apryll M Stalcup
  • 依托单位:
Novel Multimodal Selectors for CE and HPLC
  • 批准号:
    7194291
  • 项目类别:
  • 资助金额:
    $20.66万
  • 财政年份:
    2005
  • 负责人:
    Apryll M Stalcup
  • 依托单位:
PREPARATIVE ELECTROPHORETIC CHIRAL SEPARATIONS
  • 批准号:
    6127414
  • 项目类别:
  • 资助金额:
    $15.02万
  • 财政年份:
    2000
  • 负责人:
    Apryll M Stalcup
  • 依托单位:
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