12-mer peptide library screening service
Alpha Lifetech can screen high-affinity peptides quickly and efficiently for disease treatment and biological research. We offer a range of phage display peptide library construction services such as M13, T4, T7 or λ phages for our customers, with M13 phage display being our commonly used method. We are capable of constructing linear peptide libraries and structurally stable cyclic peptide libraries. Notably, We can create phage 12-mer peptide libraries with a library capacity up to 10^10 and enriched phage particles up reaching 10^13, which is conducive to screening specific antibodies with high affinity. Alpha Lifetech has a advanced phage display platform to provide the high quality phage display and screening services to clients worldwide.
Background on Peptide Library Screening
Phage 12-mer peptide library screening is to fuse a peptide gene containing 12 amino acids with the pVIII gene of a phage, and through multiple rounds of screening and enrichment, to obtain a peptide that can bind specifically to an antigen. Alpha Lifetech has a advanced phage display platform to provide the high quality phage display and screening services to clients worldwide. Our researchers have rich expertise in phage display and screening, and we can customize random peptide library construction and screening solutions to meet the needs of our clients, so that we can screen functional peptides with high affinity and specificity. We can screen the peptide libraries in a short period of time. The screened 12-mer peptide libraries can be used for vaccine development, disease diagnosis and treatment, biological research and so on.
Phage 12-mer peptide library screening Process
Alpha Lifetech offers 12-mer peptide library screening services for various targets such as antibodies, receptors, tissues, peptides and enzymes. We have developed 12-mer peptide libraries for solid-phase screening, liquid-phase screening, cell-based screening (tumor cells, primary cells), and in vivo screening in animals. The capacity of our 12-mer peptide library is up to 109, which makes it easier to screen the ideal peptide sequences due to the large library capacity. We validated the screened peptides and 98% of them have good specificity and affinity. We will go through 3 rounds of enrichment and screening of the constructed 12-mer peptide library, wash out the non-specific phage, and elute down the peptide phage that binds to the target protein. We will titer the elution products, obtain the blue and white spot plate and send it for sequencing. Finally, We analyze and deliver 10-20 peptide sequences according to customers' needs. To ensure the validity of the peptides, we can characterize the affinity of the screened 12-mer peptide, such as EC50 assay, BLI, ELISA and FACS. To ensure the functional integrity of the screened sequences, we will perform NGS validation on the screened sequences.

Fig.1 Dodecapeptide library screening process
12-mer peptide library screening Workflow
| Process | Service Content | Timeline |
|---|---|---|
| 1. Peptide Gene Design | Design of peptides containing 10-20 amino acids. | 1-2 days |
| 2. Gene Amplification And Recombinant Plasmid Construction | Amplify genes and construct on phage vectors | 1-2 weeks |
| 3. Transformation | Transform recombinant plasmids into competent cells | 2 days |
| 4. Collection of Peptide Libraries and Validation | Perform insertion rate and diversity identification | 2 days |
| 5. Peptide Library Screening | Conduct screening using solid-phase screening, liquid-phase screening, whole-cell screening, in vivo rat screening | 2-3 weeks |
| 6. Sequencing | Perform sequencing to characterize the screened peptides | 4 days |
| 7. Peptide Validation | Conduct validation assays including EC50, SPR, BLI, ELISA, FACS, NGS, cellular function validation and in vivo animal validation | 1 week |
FAQ-q&a
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1. What are the concerns about screening of 12-mer peptide libraries?
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2. How can we screen the sequences with high specificity and affinity?
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3. Can the screened 12-mer peptide be synthesized and modified?
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4. How to identify the screened 12-mer peptide sequences with complete functions?
If you have any questions, please feel free to contact us at any time.
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2018-07-16


