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Riboflavin (RF), a water-soluble vitamin, is essential for normal cellular functions and growth. During periods of dietary deprivation or physiological and pathological stress humans are vulnerable to developing RF deficiency. This results in a variety of clinical abnormalities, including growth retardation, anemia, skin lesions and degenerative changes in the nervous system. Humans cannot biosynthesize RF and, thus, must obtain the vitamin from the diet through absorption in the small intestine. Although many studies have focused on the mechanism of RF uptake, its definitive transepithelial absorption mechanism is controversial and remains to be defined in detail. Intracellular processes in RF absorption, such as cellular homeostasis, and RF function and regulation are also poorly understood. The current proposal aims to close these gaps in our knowledge of intestinal RF absorption. Our long-term objectives aim to identify, isolate, clone, and characterize the protein(s) involved in te epithelial translocation of this important vitamin. Our specific aims are: 1) Is riboflavin transported into enterocytes by a receptor- mediated and/or a carrier-mediated pathway? 2) How is RF trafficked within the cell and what is the subcellular localization of its storage compartment? 3) Is a soluble plasma RF-binding protein involved in RF translocation? Our multidisciplinary approach is designed to provide new and integrated information at the functional, cellular and molecular levels of RF transport. These studies will yield new and important information regarding a complex epithelial transport mechanism and provide important new insights in its structural specificity and function.
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A novel rhodamine-riboflavin conjugate probe exhibits distinct fluorescence resonance energy transfer that enables riboflavin trafficking and subcellular localization studies.
一种新型罗丹明-核黄素偶联探针表现出独特的荧光共振能量转移,可实现核黄素运输和亚细胞定位研究。
DOI: 10.1021/mp0499510
发表时间: 2004
期刊: Molecular pharmaceutics.
影响因子: --
作者: [Phelps,MitchA, Foraker,AmyB, Gao,Wenqing, Dalton,JamesT, Swaan,PeterW]
通讯作者: Swaan,PeterW
Riboflavin uptake in human trophoblast-derived BeWo cell monolayers: cellular translocation and regulatory mechanisms.
人滋养层来源的 BeWo 细胞单层中核黄素的摄取:细胞易位和调节机制。
DOI: --
发表时间: 2001
期刊: The Journal of pharmacology and experimental therapeutics.
影响因子: --
作者: [Huang,SN, Swaan,PW]
通讯作者: Swaan,PW
DOI: 10.1016/j.jnutbio.2006.01.008
发表时间: 2006-12
期刊: The Journal of nutritional biochemistry
影响因子: --
作者: [Vanessa M. D’Souza;Lisa Bareford;A. Ray;P. Swaan]
通讯作者: Vanessa M. D’Souza;Lisa Bareford;A. Ray;P. Swaan
Reengineering the pharmaceutical industry by crash-testing molecules.
通过对分子进行碰撞测试来重新设计制药行业。
DOI: 10.1016/s1359-6446(05)03557-9
发表时间: 2005
期刊: Drug discovery today.
影响因子: --
作者: [Swaan,PeterW, Ekins,Sean]
通讯作者: Ekins,Sean
Porous Silicon Particles for Oral Drug Delivery
  • 批准号:
    7195741
  • 项目类别:
  • 资助金额:
    $24.29万
  • 财政年份:
    2005
  • 负责人:
    PETER W SWAAN
  • 依托单位:
High-Throughput Assay for the Intestinal Peptide Transporter
  • 批准号:
    7022471
  • 项目类别:
  • 资助金额:
    $7.43万
  • 财政年份:
    2005
  • 负责人:
    PETER W SWAAN
  • 依托单位:
Porous Silicon Particles for Oral Drug Delivery
  • 批准号:
    6869204
  • 项目类别:
  • 资助金额:
    $27.08万
  • 财政年份:
    2005
  • 负责人:
    PETER W SWAAN
  • 依托单位:
Porous Silicon Particles for Oral Drug Delivery
  • 批准号:
    7011137
  • 项目类别:
  • 资助金额:
    $25.14万
  • 财政年份:
    2005
  • 负责人:
    PETER W SWAAN
  • 依托单位:
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