Modular functional peptides for the intracellular delivery of nanoparticles
Described are peptides for delivery of a nanoparticle to the cytosol, the peptide comprising: (a) a nanoparticle association domain; (b) a proline-rich spacer domain; (c) an uptake domain; and (d) a vesicle escape domain comprising a non-hydrolyzable lipid moiety, wherein the spacer domain is between the nanoparticle association domain and the uptake and vesicle escape domains, and wherein the peptide, when attached to an extracellular nanoparticle, is effective to induce uptake of the nanoparticle by a cell and delivery of the nanoparticle to the cytosol of the cell. Also described are methods of delivery of a nanoparticle to the cytosol of a cell, the method comprising providing to a cell a nanoparticle attached to such a peptide. Exemplary nanoparticles include quantum dots.
1. A peptide for delivery of a nanoparticle to the cytosol, the peptide comprising:
(a) a nanoparticle association domain;
(b) a spacer domain;
(c) an uptake domain; and
(d) a vesicle escape domain comprising a non-hydrolyzable lipid moiety or perfluoro group,
wherein said domains (a) through (d) appear in the same order as listed above, and
wherein the peptide, when attached to an extracellular nanoparticle, is effective to induce uptake of the nanoparticle by a cell and delivery of the nanoparticle to the cytosol of the cell.
2. The peptide of claim 1 , wherein the spacer domain consists of from six to fifteen proline residues.
3. The peptide of claim 1 , wherein the vesicle escape domain comprises the non-hydrolyzable lipid moiety.
4. The peptide of claim 3 , wherein said moiety is palmitoyldiamoniproprionyl.
5. The peptide of claim 1 , wherein the nanoparticle association domain comprises polyhistidine.
6. A quantum dot attached to a peptide of claim 1 .
7. A quantum dot attached to a peptide of claim 1 , wherein the peptide nanoparticle association domain comprises poly-histidine.
8. The peptide of claim 1 attached to a nanoparticle, wherein the nanoparticle is selected from the group consisting of a protein, a polymer, a dendrimer, a carbon nanotube, a rod, a sphere, a metallic particle, and combinations thereof.
9. A peptide comprising:
(a) a nanoparticle association domain comprising polyhistidine;
(b) a spacer domain comprising 8, 9, or 10 proline residues;
(c) an uptake domain comprising SEQ ID No: 7; and
(d) a vesicle escape domain comprising a non-hydrolyzable palmitic acid,
wherein said domains (a) through (d) appear in the same order as listed above.
10. The peptide of claim 9 , wherein the vesicle escape domain comprising non-hydrolyzable palmitic acid is palmitoyldiamoniproprionyl.
11. The peptide of claim 9 , wherein the spacer domain comprises 9 proline residues.
12. The peptide of claim 9 , wherein the peptide comprises SEQ ID No: 3 or SEQ ID No: 4.
13. A method of delivery of a nanoparticle to the cytosol of a cell, the method comprising providing to a cell a nanoparticle attached to a peptide according to claim 1 , and allowing the cell to take up the nanoparticle.
14. The method of claim 13 , wherein the nanoparticle is a quantum dot.
15. A method of delivery of a nanoparticle to the cytosol of a cell, the method comprising providing to a cell a nanoparticle attached to a peptide according to claim 9 , and allowing the cell to take up the nanoparticle.
16. The method of claim 15 , wherein the nanoparticle is a quantum dot.
17. A method of delivery of a nanoparticle to the cytosol of a cell, the method comprising providing to a cell a nanoparticle attached to a peptide according to claim 9 , and allowing the cell to take up the nanoparticle.
18. The method of claim 17 , wherein the nanoparticle is a quantum dot.