Analysis and engineering of receptor-mediated transcytosis across the intestinal epithelium
Analysis and engineering of receptor-mediated transcytosis across the intestinal epithelium
批准号:
9916734
负责人:
Casim Sarkar
金额:
$32.64万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2018
资助国家:
美国
项目状态:
已结题
起止时间:
2018-07-01 至 2022-04-30
关键词:
AddressBacteriaBiologicalBiological AvailabilityBlood CirculationCarrier ProteinsCellsCoculture TechniquesDevelopmentDiabetic mouseDirected Molecular EvolutionDiseaseEngineeringEnterocytesEpithelialEpithelial CellsEpitheliumEvolutionFoodGastrointestinal tract structureGeneticGenetic EngineeringHealthHumanIn VitroInsulinIntestinesLactococcus lactisLigand BindingLigandsM cellMediatingMethodsMicrobeModelingOralOral AdministrationPharmaceutical PreparationsPhenotypeProcessPropertyProteinsPublic HealthResearchSideTestingTherapeuticValidationbaseengineered stem cellshuman modelhuman pluripotent stem cellimprovedin vitro Modelin vivoinsulin secretionintestinal epitheliummicrobialmouse modelnovelnovel therapeuticsphysical separationreceptorsynthetic biologytherapeutic proteintranscytosis
中文摘要
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英文摘要
PROJECT SUMMARY
The process of receptor-mediated transcytosis is a critical, yet highly selective, mechanism for the transport of
proteins from the intestinal lumen into systemic circulation. Despite the fundamental importance of this
transport mechanism and the potential to exploit it to revolutionize oral delivery of protein therapeutics, our
understanding of intestinal transcytosis has been limited by both the lack of a more accurate, scalable in vitro
model of the human intestinal epithelium and the difficulty in identifying the full repertoire of receptors that can
actively and selectively transport cargo from the luminal side to the basolateral side of this physical barrier. In
this R01 proposal, we will synergistically integrate stem cell engineering, directed protein evolution, and
synthetic biology approaches to first uncover new mechanisms of receptor-mediated transcytosis and to then
apply these findings to create a novel platform for oral delivery of insulin. More generally, our approaches and
results should have broad utility in understanding the formation of epithelial barriers and in efficiently delivering
drugs across them in a highly selective manner.
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