Examples of 'small peptides' in a sentence
Meaning of "small peptides"
Small peptides are short chains of amino acids. Peptides are crucial building blocks of proteins and play various roles in biological processes. They can be used as therapeutics, as they can interact with specific proteins and influence biological functions in the body
How to use "small peptides" in a sentence
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small peptides
Small peptides also can be synthesized in the laboratory.
Alirocumab is expected to degrade to small peptides and individual amino acids.
Small peptides are typically unstable and are susceptible to degradation in aqueous solution.
Aflibercept is expected to degrade to small peptides and individual amino acids.
Small peptides with few amino acids are absorbed directly as such.
Dupilumab is expected to degrade to small peptides and individual amino acids.
The use of small peptides in therapeutics is preferred for various reasons.
Cemiplimab is expected to degrade to small peptides and individual amino acids.
The number of small peptides available in recombinant random libraries is enormous.
Ibalizumab is expected to degrade to small peptides and individual amino acids.
Proteases termed cathepsins degrade internalized proteins into small peptides.
Mixture of small peptides.
Small peptides are important cell signaling involved in several aspects of plant development.
Tends to be small peptides.
Some may be present in the form of amino acids and small peptides.
See also
This is particularly useful in producing small peptides and fragments of larger polypeptides.
Libraries of small peptides have also been successfully screened in vitro in assays for bioactivity.
Colostrum as such contains hundreds of small peptides which serve numerous purposes.
Straight chain lipid molecules have shown to be effective for delivering small peptides.
Small peptides have been used in the treatment of measles virus and herpes virus infections.
Human antibodies are predominately catabolized by lysosomal enzymes to small peptides and amino acids.
Model studies were undertaken with small peptides to investigate the native chemical ligation approach.
The present invention also features adaptability of use with a wide variety of small peptides.
The proteasome degrades intracellular proteins into small peptides that are then released into the cytosol.
Even small peptides without defined tertiary structure may also have specific target binding properties.
These inhibitors are generally chemical derivatives of proline or small peptides containing terminal prolines.
Mixture of small peptides according to the invention,.
She also published two books describing the cyclol theory and small peptides in general.
As a substrate, small peptides are particularly well suited.
The Fc fragment is digested into small peptides.
These drugs are small peptides displaying major properties,.
This is accomplished by a series of proteases that break Ii down into small peptides.
T lymphocytes recognize only the small peptides presented by MHC molecules.
These small peptides disrupt gonadotropin-secretion by the pituitary gland.
Many integrins can be inhibited by small peptides incorporating the RGD sequence.
Moreover, small peptides can be produced by in vitro synthetic methods and assayed.
It is presently believed that protein antigens undergo cleavage into small peptides in the APC.
Conventionally, small peptides or steroid hormones are attached to larger carrier proteins.
Examples of small molecules include small peptides or peptide-like molecules.
The conjugation hormones may be non-polar amino acids or small peptides.
Small peptides have been discovered that, like hormones, act on certain target organs.
This strategy has been used to monitor cleavage of small peptides by proteinases, e . g.
At pH 2 the small peptides and free amino acids preferentially bind themselves to the largest.
Hollow fiber module retention and up-concentration assay of two small peptides.
Defensins, originally found in mammals, are small peptides containing six to eight cysteine residues.
For the small peptides and complexes of the invention, this may prove useful.
In addition, the container should be permeable to liquids, small peptides and amino acids.
However, small peptides when unconstrained will tend to form structures which present a limited interaction surface.
For example, phage libraries displaying small peptides could be used for such selection.
The process combines solid-phase chemistry and photolithography to achieve a diverse array of small peptides.
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Opioid peptides and ORs are present in gut
Therefore a lower number of longer peptides is obtained
These peptides contain one disulphide bridge
