Virus-like particles and methods of use
The invention features modified alphavirus or flavivirus virus-like particles (VLPs). The invention provides methods, compositions, and kits featuring the modified VLPs. The invention also features methods for enhancing production of modified VLPs for use in the prevention or treatment of alphavirus and flavivirus-mediated diseases. The invention also provides methods for delivering agents to a cell using the modified VLPs.
1. An isolated polynucleotide encoding an altered viral protein selected from the group consisting of:
a. an alphavirus E2 protein comprising at least one alteration, relative to the wild-type amino acid sequence, at one or more amino acid locations corresponding to at least one amino acid position selected from the group consisting of H170, K200, K233, K234, R251, and H256 of Chikungunya E2 protein; and
b. an alphavirus capsid protein comprising at least one alteration, relative to the wild type sequence, in the Nuclear Localization Signal (NLS);
wherein the altered protein is capable of self-assembling into a virus like particle (VLP); and,
wherein the at least one alteration enhances production of VLPs.
2. The isolated polynucleotide of claim 1 , wherein the alphavirus is selected from the group consisting of Eastern equine encephalitis virus (EEEV), Western equine encephalitis virus (WEEV), Venezuelan equine encephalitis virus (VEEV), Semliki Forest virus (SFV), Chikungunya virus (CHIKV), O′nyong-nyong virus, Sindbis virus, Mayaro virus, Ross River virus, Barmah Forest virus, and Ockelbo virus.
3. The isolated polynucleotide of claim 1 , wherein the at least one alteration in the NLS is in at least one amino acid position selected from the group consisting of:
a. amino acids 67-70 of an EEEV capsid protein;
b. amino acids 67-70 of an WEEV capsid protein;
c. amino acids 64-68 of an VEEV capsid protein;
d. amino acids 62-69 of a CHIKV capsid protein;
e. amino acids 71-74 of a Ross River virus capsid protein; and
f. amino acids 64-68 of a Barmah Forest virus capsid protein.
4. The isolated polynucleotide of claim 1 , wherein the at least one alteration comprises a substitution in a charged amino acid of the NLS.
5. A kit comprising the isolated polynucleotide of claim 1 .
6. A method for producing a VLP, comprising introducing into a cell a polynucleotide encoding an altered viral protein selected from the group consisting of:
a. an alphavirus E2 protein comprising at least one alteration, relative to the wild-type amino acid sequence, at one or more amino acid locations corresponding to at least one amino acid position selected from the group consisting of H170, K200, K233, K234, R251, and H256 of Chikungunya E2 protein; and
b. an alphavirus capsid protein comprising at least one alteration, relative to the wild type sequence, in the Nuclear Localization Signal (NLS);
wherein the altered protein is capable of self-assembling into a virus like particle (VLP); and,
wherein the at least one alteration enhances production of VLPs.
7. The method of claim 6 , wherein the alphavirus or flavivirus is selected from the group consisting of Eastern equine encephalitis virus (EEEV), Western equine encephalitis virus (WEEV), Venezuelan equine encephalitis virus (VEEV), Semliki Forest virus (SFV), Chikungunya virus (CHIKV), O′nyong-nyong virus, Sindbis virus, Mayaro virus, Ross River virus, Barmah Forest virus, and Ockelbo virus.
8. The method of claim 6 , wherein the at least one alteration in the NLS is in at least one amino acid position selected from the group consisting of:
a. amino acids 6-70 of an EEEV capsid protein;
b. amino acids 67-70 of an WEEV capsid protein;
c. amino acids 64-68 of an VEEV capsid protein;
d. amino acids 62-69 of a CHIKV capsid protein;
e. amino acids 71-74 of a Ross River virus capsid protein; and
f. amino acids 64-68 of a Barmah Forest virus capsid protein.
9. The method of claim 6 , wherein the at least one alteration comprises a substitution in a charged amino acid of the NLS.