LifeTein Peptide Synthesis Service Overview
LifeTein Peptide Synthesis Service Overview
LifeTein Peptide Synthesis Service Overview
Outline
More than 60 synthetic therapeutic peptides under 50 amino acids in size have reached the pharmaceutical market as APIs or generics.
Chemical Optimization
Technology Trends
Microwave Synthesis
PeptideSynTM Platform Provides high-yield peptide synthesis Combines SPPS and LPPS for the highest synthesis success rate possible Ensures shorter turnaround
PeptideSynTM Ligation Synthesizes long peptides (up to 120 amino acids) Ensures high yield and short turnaround
LifeTein Services
Custom Peptide Synthesis Service Custom Peptide Library Synthesis Service Custom Polyclonal Antibody Service Custom Monoclonal Antibody Service
LifeTein Services
Advantages of PeptideSynTM Technology
Increases yields and reduces costs Shortens production cycle Combines the advantages of both solid and solution phase methods Can scale up projects rapidly to over 100 kg Avoids solubility problems for long segments in solution phase
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Case Studies
Cell Penetrating Peptides
Name
Tat family Tat (48-60) Oligoarginine Penetralia family p-Antp Antermapedia homeodomain RQIKIWFQNRRMKWKK HIV-1 protein Tat derivative GRKKRRQRRRPPQQ Rn
Origin
Sequence
plsl
Chimeric CPPs Transportan
Igl-1 homeodomain
RVIRVWFQNKRCKDKK
Galanin-mastoparan
GWTLNSAGYLLGKINLKALAA LAKKIL
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Case Studies
Cell Penetrating Peptides
Attached to a CPP, therapeutic cargo is delivered to an intracellular target, thus overcoming the entry restrictions set by the plasma membrane.
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Case Studies
N-Terminal Acetylation and C-Terminal Amidation
Both modifications are free of charge
N-terminal acetylation and C-terminal amidation reduce the overall charge of the peptide. This can increase the stability of the peptide and its resemblance to the native protein.
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>75% for antibody generation, >90% for phosphorylated peptide antibody (recommended)
Keep the hydrophobic amino acid content below 50% At least one charged residue for every five amino acids
Cys and Met can undergo rapid oxidation Avoid multiple Ser or Pro Avoid multiple or adjacent -sheet forming amino acids: Glu, Iso, Leu, Phe, Thr, Tyr, Val KLH, BSA, OVA
Carrier Proteins
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