Method of isolating aptamers for minimal residual disease detection

1. A method for selecting and isolating aptamers that target M-Ig proteins, comprising:

a) providing a microdevice to select and isolate M-Ig targeting oligomers comprising:

a first selection chamber for positive selection,

a second selection chamber for counter-selection, wherein the first selection chamber is connected to the second chamber via a first channel,

a third selection chamber for negative selection, wherein the second selection chamber is connected to the third selection chamber via a second channel, and

an amplification chamber, wherein the amplification chamber is connected to at least one of the first chamber, second chamber, and third chamber via a third channel, wherein the first, second, and third channels are configured to hydrodynamically and/or electrokinetically transfer a solution;

b) obtaining a first sample of M-Ig proteins from a serum;

c) placing the first sample of M-Ig proteins in the first selection chamber;

d) placing a second sample of M-Ig or polyclonal immunoglobulin proteins having a heavy and light chain substantially similar to the first sample of M-Ig proteins in the second selection chamber;

e) placing beads without a molecular coating in the third selection chamber;

f) introducing a first group of oligomers including at least an M-Ig targeting oligomer into the first selection chamber, whereby the M-Ig targeting oligomer binds to the first sample of M-Ig proteins;

g) removing unbound oligomers from the first selection chamber to isolate the M-Ig targeting oligomer;

h) transferring the M-Ig targeting oligomer to the second selection chamber, whereby an unbound oligomer is counter-selected;

i) transferring the counter-selected unbound oligomer to the third selection chamber, whereby a subsequent unbound oligomer is negatively selected from the counter-selected unbound oligomer;

j) transferring the subsequent unbound M-Ig targeting oligomer to the amplification chamber through the second channel by a pressure-driven or electrokinetic-driven flow; and

k) amplifying the M-Ig targeting oligomer in the amplification chamber by polymerase chain reaction.

2. The method of claim 1 , wherein the obtaining of the first sample of M-Ig proteins comprises gel electrophoresis; and isoelectric focusing.

3. The method of claim 1 , further comprising purifying the M-Ig proteins using affinity purification after the obtaining of the first sample of M-Ig proteins.

4. The method of claim 3 , wherein the affinity purification comprises using a immunoglobulin specific recombinant bacterial binding protein.

5. The method of claim 1 , wherein the first selection chamber comprises microbeads functionalized with a target M-Ig protein, wherein the method further comprises immobilizing the first sample of M-Ig proteins on the microbeads in the first selection chamber.

6. The method of claim 5 , wherein the microbeads comprise N-hydroxysuccinimde (NHS) groups functionalized magnetic beads to immobilize the M-Ig proteins.

7. The method of claim 1 , wherein the amplification chamber comprises primer-functionalized magnetic beads configured to capture the M-Ig targeting oligomer.

8. The method of claim 1 , further comprising forming the first selection chamber, the second selection chamber, the third selection chamber, and the amplification chamber on a microchip.

9. The method of claim 8 , further comprising hydrodynamically or electrokinetically transferring the M-Ig targeting oligomer from the amplification chamber to the first selection chamber.