Peptide libraries, which contain a number of peptides consisting of a series of amino acids, are a new approach to the study of protein structure and function. They provide a rapid and cost-effective solution to identify key bioactive peptides for a wide range of bioactivity screening purposes and have widely used in biological research. Peptide library has become a powerful tool in biochemistry and drug applications. Due to the growing interest in peptide drugs, the demand for peptide libraries from pharmaceutical companies continues to grow.
With over 25 years of experience in the design and production of custom peptide libraries, BOC Sciences, a team of professionals, is committed to providing high-quality peptide library services at a very competitive prices using our accumulated knowledge and experience in synthetic chemistry.
Figure 1. Schematic presentation of constructing the CX7C-peptide library. (Baalen, A. V., Stephani, U. 2002)
Figure 2. Illustration of the on-chip screening for peptide-based protein binders. (Schwaar, T.; et al. 2019)
BOC Sciences provides advice on creating the most efficient and cost-effective library design, offering a range of library design options:
We apply 20 natural amino acids to randomly and simultaneously substitute the selected residues of a peptide sequences using a ‘shotgun approach’ to create our random peptide libraries.
Our experienced experts divide the original protein or peptide sequence into many overlapping peptides of the same length to generate an overlapping peptide libraries. We fully consider peptide length and peptide offset that play important role in the library construction.
In order to build an alanine scanning peptide library, we use alanine to substitute the residues at each amino acid position of the original peptide, which can generate alanine with less or no binding or activity.
We use natural amino acids to replace one or more selected residues within a peptide sequence. The amino acids we apply can increase activity or binding and can be identified using a positional scanning library.
Aiming find the minimum length of an epitope, BOC Sciences can deliver a scrambled library by reducing the peptide length of amino acid from each terminus creating a set of truncated peptides with different lengths.
At BOC Sciences, we create a reliable scrambled library via permutation of the original peptide sequence and represents all alternative peptides with the same amino acid composition.
Our well-developed T-cell truncated peptide library is composed of truncated peptide combinations to ensure that the entire T-cell epitope can be spanned across structural domains
We establish a micro-scale peptide library that is composed of multiple peptides containing systematic combinations of amino acids to offer peptides at micromolar scales. Our unique library is an optimal choice for targeted proteomics applications and preliminary screening.
BOC Sciences supports a variety of cyclization strategies to synthesize peptides such as head-to-tail cyclization, side-chain-to-side-chain, head-to-side-chain, and side-chain-to-tail cyclization.
As a complement to our peptide library service, we have developed multiple pools of peptides for the accurate stimulation of T-cells. We can prepare customized peptide pools according to your customized specifications with pre-pooling LC-MS validation, and post-pooling marker validation QC options.
BOC Sciences has introduced an advanced peptide HTS library synthesis platform, to synthesize high throughput peptides with industry leading speed and flexibility.
BOC Sciences provides professional, rapid and high-quality services of Peptide Library design at competitive prices for global customers. Personalized and customized services of Peptide 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!
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BOC Sciences has rich experience in working with global customers in custom library synthesis of compounds and generating small to medium-sized libraries of target compounds. Our knowledge in generating a large number of target molecules in a remarkably shorter time enables quick biological screenings for affinities. With the target properties in mind, we deliver target molecules, by applying our extensive knowledge in drug discovery.