Table 1.
Architectures and assemblies of ELP drug carriers
Application | ELP sequence | Pertinent functionalization | Ref |
---|---|---|---|
Recombinant protein purification | (VPGXG)36 X=K1V7F1 | Cecropin AD antimicrobial peptide with enterokinase cleavage site | [31] |
(VPGXG)90 X=V5A2G3 | Halocidin18 antimicrobial peptide with hydroxylamine cleavage site | [34] | |
(VPGXG)110 X=V5A2G3 | Moricin CM4 and human β-defensin 4 antimicrobial peptides with intein cleavage sites | [37] | |
(VPGVG)240 | SrtA transpeptidase for site-specific cleavage and triglycine addition | [38] | |
(VPGXG)90 X=A2G3V5 | TNFα and TRAIL apoptosis-inducing cytokines with SrtA cleavage sites | ||
Therapeutic protein ELP fusions | (VPGXG)90 X=V5G3A2 | IL-1ra anti-inflammatory cytokine | [39] |
(VPGVG)27 | IL-4 and IL-10 anti-inflammatory cytokines | [19, 40] | |
(VPGVG)n n=5–240 | IL-10 anti-inflammatory cytokine and EPO hematopoietic cytokine | [17] | |
(VPGXG)100 X=V, G, or A | HIV neutralizing antibody | [41] | |
(VPGXG)100 X=V5G3A2 | TNF-VHH inhibitor for prevention of septic shock | [18] | |
Targeted peptide ELP fusions | [AP1-(VGVPG)12]6 | AP1 peptide for tumor homing to IL-4 receptor | [42] |
(VPGXG)120 X=V1G7A8 | TAT, MTS, and penetratin CPPs for enhanced cellular uptake and intracellular delivery of p21 peptide drug | [43] | |
Therapeutic small molecule drug ELP conjugates | (VPGXG)150 X=V5A2G3 and (VPGXG)160 X=V1A8G7 | Lysine residue for conjugation of chemotherapeutic doxorubicin with acid-cleavable hydrazone linker | [44] |
(VPGXG)180 X=V5A2G3 | Cysteine residue for conjugation of chemotherapeutic doxorubicin with acid-cleavable hydrazone linker | [45] | |
(VPGXG)150 X=V5A2G3 and (VPGXG)160 X=V1A8G7 | Cysteine residue for conjugation of chemotherapeutic doxorubicin with enzyme-cleavable peptide linker and TAT CPP for enhanced cellular uptake | [46] | |
Block copolymer ELP assemblies | (VPGXG)96 [X=V1A8G7]-(VPGVG)60 | RGD and NGR peptide at hydrophilic terminus for multivalent display of ligands for receptors on tumor vasculature | [47] |
(VPGXG)64 [X=V1A8G7]-(VPGVG)90 | NGR peptide at hydrophilic terminus for multivalent display of ligand for CD13 receptors on tumor vasculature | [48] | |
(VPGSG)48-(VPGIG)48 | Knob protein at hydrophilic terminus for multivalent display of CAR ligand | [49] | |
FKBP protein at hydrophilic terminus for rapamycin drug binding | [50, 51] | ||
Conjugation-driven ELP assemblies | (VPGXG)160 X=V1A8G7 | (GGC)8 peptide for conjugation of chemotherapeutic doxorubicin | [52] |
C(GGC)7 peptide for conjugation of chemotherapeutic paclitaxel | [53] | ||
ELP polyplexes | (VPGXG)60 X=V5A2G3 | K8 cationic peptide for ionic complexation with GFP-encoding plasmid DNA | [54] |
Coacervate ELP nanoparticles | (VPAVG)220 | Physical encapsulation of BMP-2 and BMP-14 cytokines for promotion of bone growth | [55] |
[VG-(VPGVG)4-VPG]8-[VG-(VPGVG)2-VPGCG-VPGVG-VPG]2 | KGF protein for promotion of wound healing | [56] | |
Cross-linked ELP particles | [(VPGVG)4-(VPGKG)]8-(VPGVG)40 | Lysine residues for glutaraldehyde cross-linking of solid microparticles with physical loading of model drugs BSA and prednisone acetate | [57] |
[(VPGVG)14-(VPGKG)]8-(VPGVG)40 | Lysine residues for glutaraldehyde cross-linking of core-shell microparticles with physical loading of model drugs rhodamine B, FITC, and rhodamine-BSA | [58] | |
EP20–244 (composed of exons from human elastin: 20-(21-23-24)4) | Lysine and glutamine residues for transglutaminase cross-linking of hollow spheres with physical loading of plasmid DNA polyplexes | [59] |