Predicting the Loading of Virus-Like Particles with Fluorescent Proteins

W.F. Rurup, F. Verbij, M.S.T. Koay, Christian Blum, Vinod Subramaniam, Jeroen Johannes Lambertus Maria Cornelissen

Research output: Contribution to journalArticleAcademicpeer-review

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Abstract

The virus-like particle (VLP) of the Cowpea Chlorotic Mottle Virus (CCMV) has often been used to encapsulate foreign cargo. Here we show two different rational design approaches, covalent and noncovalent, for loading teal fluorescent proteins (TFP) into the VLP. The covalent loading approach allows us to gain control over capsid loading on a molecular level. The achieved loading control is used to accurately predict the loading of cargo into CCMV VLP. The effects of molecular confinement were compared for the differently loaded VLPs created with the covalent method. We see that the loading of more than 10 fluorescent proteins in the 18 nm internal cavity of the CCMV capsid gives rise to a maximum efficiency of homo-FRET between the loaded proteins, as measured by fluorescence anisotropy. This shows that already at low levels of VLP loading molecular crowding starts to play a role.
Original languageUndefined
Pages (from-to)558-563
Number of pages6
JournalBiomacromolecules
Volume15
Issue number2
DOIs
Publication statusPublished - 2014

Keywords

  • IR-94969
  • METIS-306434

Cite this

Rurup, W.F. ; Verbij, F. ; Koay, M.S.T. ; Blum, Christian ; Subramaniam, Vinod ; Cornelissen, Jeroen Johannes Lambertus Maria. / Predicting the Loading of Virus-Like Particles with Fluorescent Proteins. In: Biomacromolecules. 2014 ; Vol. 15, No. 2. pp. 558-563.
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Predicting the Loading of Virus-Like Particles with Fluorescent Proteins. / Rurup, W.F.; Verbij, F.; Koay, M.S.T.; Blum, Christian; Subramaniam, Vinod; Cornelissen, Jeroen Johannes Lambertus Maria.

In: Biomacromolecules, Vol. 15, No. 2, 2014, p. 558-563.

Research output: Contribution to journalArticleAcademicpeer-review

TY - JOUR

T1 - Predicting the Loading of Virus-Like Particles with Fluorescent Proteins

AU - Rurup, W.F.

AU - Verbij, F.

AU - Koay, M.S.T.

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AU - Subramaniam, Vinod

AU - Cornelissen, Jeroen Johannes Lambertus Maria

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N2 - The virus-like particle (VLP) of the Cowpea Chlorotic Mottle Virus (CCMV) has often been used to encapsulate foreign cargo. Here we show two different rational design approaches, covalent and noncovalent, for loading teal fluorescent proteins (TFP) into the VLP. The covalent loading approach allows us to gain control over capsid loading on a molecular level. The achieved loading control is used to accurately predict the loading of cargo into CCMV VLP. The effects of molecular confinement were compared for the differently loaded VLPs created with the covalent method. We see that the loading of more than 10 fluorescent proteins in the 18 nm internal cavity of the CCMV capsid gives rise to a maximum efficiency of homo-FRET between the loaded proteins, as measured by fluorescence anisotropy. This shows that already at low levels of VLP loading molecular crowding starts to play a role.

AB - The virus-like particle (VLP) of the Cowpea Chlorotic Mottle Virus (CCMV) has often been used to encapsulate foreign cargo. Here we show two different rational design approaches, covalent and noncovalent, for loading teal fluorescent proteins (TFP) into the VLP. The covalent loading approach allows us to gain control over capsid loading on a molecular level. The achieved loading control is used to accurately predict the loading of cargo into CCMV VLP. The effects of molecular confinement were compared for the differently loaded VLPs created with the covalent method. We see that the loading of more than 10 fluorescent proteins in the 18 nm internal cavity of the CCMV capsid gives rise to a maximum efficiency of homo-FRET between the loaded proteins, as measured by fluorescence anisotropy. This shows that already at low levels of VLP loading molecular crowding starts to play a role.

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