High-throughput system and method for the temporary permeabilization of cells using lipid bilayers
A microfluidic device is disclosed that is used to process cells for the intracellular delivery of molecules or other cargo. The device includes one or more microchannels disposed in a substrate or chip and is fluidically coupled to an inlet configured to receive a solution containing the cells and the molecules or other cargo to be delivered intracellularly to the cells. Each of the one or more microchannels has one or more constriction regions formed therein, wherein the inner surface(s) of the microchannels and the one or more constriction regions have a lipid bilayer disposed thereon. In some embodiments, multiple microfluidic devices operating in parallel are used to process large numbers of cells. The device and method have particularly applicability to delivering gene-editing molecules intracellularly to cells.
1. A microfluidic device for processing cells comprising:
one or more microchannels disposed in a substrate or chip and fluidically coupled to an inlet configured to receive a solution containing the cells along with molecules or other cargo to be delivered intracellularly to the cells, each of the one or more microchannels containing a constriction region therein having a width within the range of about 4 μm to about 10 μm, wherein the one or more microchannels and the respective constriction regions have a lipid bilayer formed on internal surfaces thereof.
2. The microfluidic device of claim 1 , the substrate or chip further comprising a second inlet fluidically coupled to the one or more microchannels, wherein the second inlet is coupled to a second pump configured to pump a solution containing the molecules or other cargo to be intracellularly delivered into the cells.
3. The microfluidic device of claim 1 , wherein the one or more microchannels comprises a plurality of microchannels disposed in the substrate or chip.
4. The microfluidic device of claim 1 , wherein the lipid bilayer is positively charged.
5. The microfluidic device of claim 1 , wherein the lipid bilayer is negatively charged.
6. The microfluidic device of claim 1 , wherein the lipid bilayer is uncharged or substantially uncharged.
7. The microfluidic device of claim 1 , wherein the lipid bilayer is zwitterionic.
8. The microfluidic device of claim 1 , wherein the lipid bilayer comprises phospholipid 1,2-dioleoyl-sn-glycero-3-phosphocholine (DOPC).
9. The microfluidic device of claim 1 , wherein the lipid bilayer comprises 1,2-bis[10-(2′,4′-hexadienoyloxy) decanoyl]-sn-glycero-3-phosphocholine (bis-SorbPC).
10. A system for processing cells comprising one or more microfluidic devices of claim 1 , further comprising one or more pumps configured to simultaneously pump a solution containing the cells and the molecules or other cargo to be intracellularly transported into the cells through the one or more microfluidic devices.
11. A method of using the microfluidic device of claim 1 , comprising:
flowing in the one or more microchannels a solution containing the cells and the molecules or other cargo to be intracellularly delivered into the cells.
12. The method of claim 11 , wherein the molecules or other cargo comprise gene-editing biomolecules.
13. The method of claim 11 , wherein the gene-editing biomolecules comprise clustered regularly interspaced short palindromic repeats (CRISPR)-Cas9 biomolecules including ribonucleoprotein-guide RNA complexes and donor template DNA.
14. The method of claim 11 , wherein the one or more microchannels remain unclogged after passage of 1×10 6 cells through the plurality of microchannels.
15. A method of delivering gene-editing molecules to cells comprising:
flowing a solution containing the cells and the gene-editing molecules through one or more microchannels formed in a microfluidic device or chip, wherein each of the one or more microchannels comprises one or more constriction regions having a width within the range of about 4 μm to about 10 μm, and wherein the one or more microchannels and the one or more constriction regions comprise an internal surface or surfaces having a lipid bilayer disposed thereon.
16. The method of claim 15 , wherein the gene-editing molecules are packaged into nanoparticle carriers.
17. The method of claim 15 , wherein the lipid bilayer is positively charged.
18. The method of claim 15 , wherein the lipid bilayer is negatively charged.
19. The method of claim 15 , wherein the lipid bilayer is uncharged or substantially uncharged.
20. The method of claim 15 , wherein the lipid bilayer is zwitterionic.
21. The method of claim 15 , wherein the lipid bilayer comprises phospholipid 1,2-dioleoyl-sn-glycero-3-phosphocholine (DOPC).
22. The method of claim 15 , wherein the lipid bilayer comprises 1,2-bis[10-(2′,4′-hexadienoyloxy) decanoyl]-sn-glycero-3-phosphocholine (bis-SorbPC).
23. A method of forming a lipid bilayer on the surfaces of one or more microchannels;
providing a microfluidic device having one or more microchannels including a constriction region having a width within the range of about 4 μm to about 10 μm, the one or more microchannels comprising one or more hydrophilic surfaces; and
flowing lipid bicelles into the one or more microchannels formed using a long-chain phospholipid component and a short-chain phospholipid component, wherein the lipid bicelles naturally interact with the one or more hydrophilic surfaces of the one or more microchannels and rupture liberating the short-chain phospholipid component to form a lipid bilayer comprising the long-chain phospholipid component that conformally coats the one or more hydrophilic surfaces.
24. The method of claim 23 , wherein the long-chain phospholipid component comprises phospholipid 1,2-dioleoyl-sn-glycero-3-phosphocholine and the short-chain phospholipid component comprises 1,2-dihexanoyl-sn-glycero-3-phosphocholine (DHCP).
25. The method of claim 23 , wherein the lipid bilayer comprising the long-chain phospholipid component conformally coats the constriction region.