Peptide Cyclization Library
                    
                    
                    Cyclization modifications can confer several  advantages to peptides that cumulatively make them more drug-like. Constraining  peptides via cyclization is a common strategy to mimic (protein) secondary  structures (e.g. peptide rings) or to create peptides with enhanced  conformational stability (compared to their linear analogs).
Aiming  to construct a top-quality -peptide cyclization library, BOC Sciences has established several reaction platforms  to create various types of conformationally-constrained peptides with robust  reactions and high yields.
Application
- Discovery  of peptides with desirable stability
- Mimic  secondary protein structures (e.g. protein loops)
- Optimization of peptides, e.g. peptide  ligands with enhanced binding potency/selectivity and protease stability
 Figure 1. One step cleavage and cyclization of  unprotected peptides with the KAHA ligation.  (Florian, R.; et al.  2015)
  Figure 1. One step cleavage and cyclization of  unprotected peptides with the KAHA ligation.  (Florian, R.; et al.  2015)
Peptide  Cyclization Reaction Platform
- Cyclization  of solid-phase-synthesized peptides in solutions and on resins
- Cyclization of in vitro translated mRNA-peptide fusion  libraries on oligonucleotide (dT) resins
Our  Strategy
- Cys-Cys  cyclization
- Cys-Cys cyclization is our most commonly  applied method of peptide cyclization, where a disulfide (S-S) bond is formed  between the thiol side chains of two cysteine residues in the peptide
- We address the problem of dimerization by conducting  cyclization at high dilution conditions
- Backbone-cyclization  (amide bond formation)
- At BOC Sciences, backbone-amide cyclized  peptides are prepared by head-to-tail cyclization or side-chain-to-side chain  cyclization
- Our extensive experience and expertise in  amidocyclic peptide synthesis strategies can minimize undesired side reactions,  such as racemization or peptide capping by coupling reagents
- We are able to provide effective head-to-tail  cyclization services using optimal cyclization reagents and cyclization  conditions
- Thioether  cyclization
What  we Deliver?
- At BOC Sciences, peptide arrays are  provided in a variety of sizes and formats according to the demand of different  projects
- Peptide lengths can  be ranging from 5 to 30 amino acids, which can meet most requirement of applications
- Our expert teams  can provide peptide library containing up to 50 amino acid if there is special  demand
- Standard delivery  times of around 3-4 weeks depending on different library size and peptide  length
- Delivered as  freeze-dried in 96-well plates for subsequent experiments
- Analytical MS and  HPLC data are available for each peptide product
- BOC Sciences offers standard TFA removal service according to the customer's requirements
BOC Sciences provides professional,  rapid and high-quality services of Peptide Cyclization Library design at  competitive prices for global customers. Personalized and customized services  of Peptide Cyclization Library design can satisfy any innovative scientific  study demands. Our clients have direct access to our staff and prompt feedback  to their inquiries. If you are interested in our services, please contact us immediately!
Reference
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			Florian, R.; et al. Spontaneous  head-to-tail cyclization of unprotected linear peptides with the KAHA ligation. Chemical Science.  2015. 6(8): 4889-4896.