Review Article

Postexit Surface Engineering of Retroviral/Lentiviral Vectors

Table 1

Approaches to post-exit modification of R/LV vector surfaces.

TypeVirus/vectorModificationObjectiveReferences

Covalent chemical
 Iodination(AV), VSV, RVRadionuclidesL[8]
 Reductive aminationRVLactoseR[9]
 ConjugationLVPoly (ethylene) glycolH[10]
 BiotinylationRV, HVBiotin, different secondaryR[11, 12]
 PAL chemistry*RVBiotin, Alexa fluorophoreP, L[13]
Membrane-topic
 FSLVSV, MV, IVFluorescein, BiotinL[14]
 Molecular paintingRV, LV, HV, IVCD59, GFPL, H[7, 15]
 Membrane-traversing**HVRadionuclidesL[16]
 Synthetic GPI**n.a.n.a.n.a.[17]
 Oleyl/PEG**n.a.Streptavidin, GFP, mABL[18]
 Myristyl/peptide**n.a.CD59(H)[19]
Adaptor-based
  (Strept)avidin (soluble)RVStreptavidin, MHCR[20]
  (Strept)avidin (membr.)***LV, BVBiotinylated radionuclids, antibodies and ligandsL, R[4]
 BiotinylationSee above
 Biotin acceptor peptide***LV, BVBiotin, different secondaryP, R[2124]
 Bridging moleculesRV, HVHeregulin
EGF, VEGF
AntiCEA
R[2528]
 Bispecific antibodies**(AV)AntiCD40
AntiEndoglin
R, H[29, 30]
 Antibody binding (membr.)***RVAntiHER2
AntiP-GP
R[31, 32]
 “Clickable” Adaptors**(AV)TAMRA(L)[33]
 Split inteins**/***n.a.GFP(L)[34]

Mostly pre-exit, **not tried on R/LV, ***requires genetic modifications (transfection/transduction) to deliver part of the system. RV: retrovirus, LV: lentivirus, VSV: vesicular stomatitis virus, MV: measles virus, IV: influenza virus, HV: herpes virus, BV: baculovirus, AV: adenovirus. Lenti/retroviruses are in bold and underlined, viruses in brackets are naked viruses. P: preparation, L: labeling, H: host responses, R: range of infectivity. Objectives in brackets have not been carried out on enveloped viruses. CD59 protectin, GFP green fluorescent protein, MHC major histocompatibility complex, EGF epidermal growth factor, VEGF vascular endothelial growth factor, CEA carcinoembryonic antigen, HER human epidermal growth factor receptor 2, P-GP permeability glycoprotein, TAMRA Carboxytetramethylrhodamine.