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DESCRIPTION (provided by applicant): Phage display is an extraordinarily powerful and versatile technology that enables the selection of novel binding functions from large populations of randomly generated peptide sequences. From a sufficiently complex library, phage bearing peptides with practically any desired binding activity can be physically isolated by affinity selection, and, since each particle carries in its genome the genetic information for its own replication, the selectants can be amplified in bacteria. This aim of this project is to develop a new platform for peptide display on virus-like particles (VLPs) of the RNA bacteriophage MS2. We envision several applications for the MS2 VLP, but we wish especially to emphasize its utility for vaccine development. It will integrate into a single platform the potent immunogenicity of a VLP with the affinity selection capability of conventional phage display. Filamentous phages are now the most widely used vehicles for phage display, and provide an efficient means for epitope identification. However, the peptides they display are typically poorly immunogenic, because they do not normally support the formation of dense repetitive arrays. Meanwhile, other VLP systems permit engineered display of specfic pre-selected epitopes, but are incapable of peptide library display and affinity selection. We think MS2 VLPs will overcome these limitations. Peptides displayed on MS2 VLPs are strongly immunogenic, and can be engineered to encapsidate the same mRNA molecule that encodes them, thus enabling recovery of affinity selected sequences by RT-PCR. Further, the comparative simplicity of MS2 VLP structure and assembly makes it possible to conduct the entire iterative selection/amplification process in vitro. This could make it easier to achieve high library complexities, and should make automation possible. PUBLIC HEALTH RELEVANCE: This project aims to develop a new platform for peptide display using virus-like particles of bacteriophage MS2. Several applications are envisioned, but because of their potent immunogenicity, these particles should be especially useful for vaccine discovery.
期刊论文(11)
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会议论文
DOI: 10.1016/j.coviro.2016.03.001
发表时间: 2016-06
期刊: Current opinion in virology
影响因子: 5.9
作者: [Frietze KM, Peabody DS, Chackerian B]
通讯作者: Chackerian B
DOI: 10.1186/1477-3155-9-22
发表时间: 2011-05-24
期刊: Journal of nanobiotechnology
影响因子: 10.2
作者: [Caldeira JC, Peabody DS]
通讯作者: Peabody DS
DOI: 10.1371/journal.pone.0141407
发表时间: 2015
期刊: PloS one
影响因子: 3.7
作者: [Caldeira J, Bustos J, Peabody J, Chackerian B, Peabody DS]
通讯作者: Peabody DS
DOI: 10.1021/nn201397z
发表时间: 2011-07-26
期刊: ACS nano
影响因子: 17.1
作者: [Ashley CE, Carnes EC, Phillips GK, Durfee PN, Buley MD, Lino CA, Padilla DP, Phillips B, Carter MB, Willman CL, Brinker CJ, Caldeira Jdo C, Chackerian B, Wharton W, Peabody DS]
通讯作者: Peabody DS
RNA-BINDING SITE OF A TRANSLATIONAL REPRESSOR
  • 批准号:
    2181728
  • 项目类别:
  • 资助金额:
    $13.88万
  • 财政年份:
    1991
  • 负责人:
    David S. Peabody
  • 依托单位:
RNA BINDING SITE OF A TRANSLATIONAL REPRESSOR
  • 批准号:
    2857129
  • 项目类别:
  • 资助金额:
    $18.56万
  • 财政年份:
    1991
  • 负责人:
    David S. Peabody
  • 依托单位:
GENETIC ANALYSIS OF A TRANSLATIONAL REPRESSOR
  • 批准号:
    3301840
  • 项目类别:
  • 资助金额:
    $12.49万
  • 财政年份:
    1991
  • 负责人:
    David S. Peabody
  • 依托单位:
Genetic Analysis of a Translational Repressor
  • 批准号:
    7228716
  • 项目类别:
  • 资助金额:
    $3.61万
  • 财政年份:
    1991
  • 负责人:
    David S. Peabody
  • 依托单位:
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