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PDBsum entry 4zor

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protein ligands Protein-protein interface(s) links
Virus PDB id
4zor

 

 

 

 

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Contents
Protein chains
128 a.a.
Ligands
PO4 ×4
Waters ×432
PDB id:
4zor
Name: Virus
Title: The structure of the s37p ms2 viral capsid assembly.
Structure: Coat protein. Chain: a, b, c, d, e. Engineered: yes. Mutation: yes
Source: Enterobacteria phage ms2. Organism_taxid: 329852. Expressed in: escherichia coli k-12. Expression_system_taxid: 83333
Resolution:
2.20Å     R-factor:   0.219     R-free:   0.243
Authors: M.A.Asensio,B.Sankaran,P.H.Zwart,D.Tullman-Ercek
Key ref: M.A.Asensio et al. (2016). A Selection for Assembly Reveals That a Single Amino Acid Mutant of the Bacteriophage MS2 Coat Protein Forms a Smaller Virus-like Particle. Nano Lett, 16, 5944-5950. PubMed id: 27549001 DOI: 10.1021/acs.nanolett.6b02948
Date:
06-May-15     Release date:   07-Sep-16    
PROCHECK
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 Headers
 References

Protein chains
P03612  (CAPSD_BPMS2) -  Capsid protein from Escherichia phage MS2
Seq:
Struc:
130 a.a.
128 a.a.*
Key:    Secondary structure  CATH domain
* PDB and UniProt seqs differ at 1 residue position (black cross)

 

 
DOI no: 10.1021/acs.nanolett.6b02948 Nano Lett 16:5944-5950 (2016)
PubMed id: 27549001  
 
 
A Selection for Assembly Reveals That a Single Amino Acid Mutant of the Bacteriophage MS2 Coat Protein Forms a Smaller Virus-like Particle.
M.A.Asensio, N.M.Morella, C.M.Jakobson, E.C.Hartman, J.E.Glasgow, B.Sankaran, P.H.Zwart, D.Tullman-Ercek.
 
  ABSTRACT  
 
Virus-like particles are used to encapsulate drugs, imaging agents, enzymes, and other biologically active molecules in order to enhance their function. However, the size of most virus-like particles is inflexible, precluding the design of appropriately sized containers for different applications. Here, we describe a chromatographic selection for virus-like particle assembly. Using this selection, we identified a single amino acid substitution to the coat protein of bacteriophage MS2 that mediates a uniform switch in particle geometry from T = 3 to T = 1 icosahedral symmetry. The resulting smaller particle retains the ability to be disassembled and reassembled in vitro and to be chemically modified to load cargo into its interior cavity. The pair of 27 and 17 nm MS2 particles will allow direct examination of the effect of size on function in established applications of virus-like particles, including drug delivery and imaging.
 

 

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