Tagged ligands for enrichment of rare analytes from a mixed sample
View Patent ↗Method of enriching specific cells from cellular samples are disclosed, comprising contacting in solution a cellular sample with affinity-tagged ligands (ATLs) each comprising a first ligand linked to an affinity tag, wherein the ligand selectively binds a cellular marker of the rare cells and the affinity tag can be selectively captured by a capture moiety, wherein the affinity tags do not comprise a magnetic particle; and flowing the sample through a microfluidic device comprising the capture moiety to selectively retain ATL-bound cells. Methods for enriching circulating tumor cells, and devices for enriching specific cells from cellular samples are also disclosed.
1. A method for enriching rare cells from a cellular sample comprising:
(a) contacting in solution said cellular sample with affinity-tagged ligands (ATLs) each ATL comprising:
a first ligand linked to an affinity tag, wherein said ligand selectively binds a cellular marker of said rare cells, said affinity tag can be selectively captured by a capture moiety, and said affinity tag does not comprise a magnetic particle; and
(b) flowing said cellular sample containing said ATLs through a microfluidic device comprising a substrate coated with said capture moiety to thereby selectively retain ATL-bound cells by binding said affinity tag to said capture moiety.
2. The method of claim 1 , wherein said rare cells are circulating tumor cells or epithelial cells.
3. The method of claim 1 , wherein said ligand is folic acid, epidermal growth factor (EGF), Dolichos Biflorus Agglutinin (DBA), EGF peptide, epi peptide, transforming growth factor-alpha (TGF-alpha), Urokinase Plasminogen Activator (UPA), FasL, MUC1/sec, catenin, ICAM-1, or plasminogen.
4. The method of claim 1 , wherein said ligand is an antibody.
5. The method of claim 4 , wherein said antibody is anti-EpCam, anti-ErbB2, or anti-CK19 antibody.
6. The method of claim 1 , wherein said ligand is not an antibody.
7. The method of claim 1 , wherein said affinity tag is biotin, desthiobiotin, histidine, polyhistidine, myc, hemagglutinin (HA), FLAG, fluorescence tag, tandem affinity purification (TAP) tags, or glutathione S transferase (GST) or derivatives thereof.
8. The method of claim 1 , wherein said ATLs comprises: (a) a first ATL comprising a first ligand that selectively binds a first cellular marker of the rare cells., wherein said first ligand is linked to a first affinity tag, and (b) a second ATL comprising a second ligand that selectively binds a second cellular marker of the rare cells, wherein said second ligand is linked to a second affinity tag, wherein the first ligand and the second ligand are different.
9. The method of claim 1 , wherein said ATLs comprises at least 3, 4, 5, 6, 7, or 8 different ATLs, each comprising a ligands, which selectively binds a different cellular marker of the rare cells.