Methods and systems for detecting and/or sorting targets
A target and sample detection technology, which is applied in the field of detection and/or sorting targets and systems, can solve problems such as sampling errors, and achieve the effects of improving sensitivity and minimizing protein denaturation
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Embodiment 1
[0154] Example 1: Production of Antibodies Encoded by Polynucleotides
[0155] according to figure 1 The two-step strategy shown produces antibodies encoded in DNA. Specifically, aldehyde functional groups were introduced into 5-aminated oligonucleotides via succinimide chemistry using commercially available reagents ( figure 1 Figure a). Similarly, the hydrazide moiety was introduced by reaction with the lysine side chain in the corresponding antibody ( figure 1 Figure a). DNA-antibody conjugate formation is then facilitated by stoichiometric hydrazone bond formation between the aldehyde and hydrazide functional groups. Verify conjugate formation by PAGE electrophoresis and control for DNA loading ( figure 1 Figure b).
[0156] For these experiments polyclonal goat anti-human IgG labeled with AlexaFluor 488, 594 and 647 were purchased from Invitrogen. Monoclonal rabbit anti-human interleukin-4 (clone 8D4-8), non-fluorescent and APC-labeled rabbit anti-human TNF-α (clon...
Embodiment 2
[0165] Example 2: Production of polynucleotide-encoded streptavidin
[0166] Production of DNA-encoded streptavidin was performed according to the same route described in Example 1 for the production of DNA-encoded antibodies. The only difference is that the SANH:streptavidin ratio was kept constant at 100:1.
Embodiment 3
[0167] Example 3: Optimizing the polynucleotide load of a polynucleotide-encoded antibody
[0168] Unfavorable steric effects when labeling antibodies with oligonucleotides are considerations when performing various assays, such as the immunoassays and cell sorting / capture experiments described herein. To this end, the ability of DNA-encoded antibodies to retain cell surface markers, visualized by fluorescence-activated cell sorting (FACS), was investigated. DNA loading was optimized using FACS for polynucleotide-encoded conjugates by using a fluorophore covalently labeled on the DNA instead of the antibody. For this analysis, 5′-aminated, 3′-FITC-labeled DNA was labeled with different stoichiometric ratios of SANH to antibody (5:1, 25:1, 50:1, 100:1, 300:1) in Anti-CD90.2 antibody on. This produced on average conjugates with 1, 2, 3, 4-5 and 6-7 FITC-DNA strands, respectively, as measured by gel mobility assay, see figure 1 Figure d. The ability of these conjugates to bin...
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