Examples of 'non-natural amino' in a sentence
Meaning of "non-natural amino"
Non-natural amino acids are synthetic molecules that are structurally similar to natural amino acids, but with modified or additional functional groups. They are often used in research and drug development to study protein structure and function. Non-natural amino acids can also be incorporated into proteins through genetic engineering techniques
How to use "non-natural amino" in a sentence
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non-natural amino
Variants may comprise non-natural amino acids.
The non-natural amino acid may comprise a saccharide moiety.
Aromatic rings of a non-natural amino acid include.
The non-natural amino acid polypeptide may be produced in vitro.
Methods and compositions comprising non-natural amino acids.
Further examples of non-natural amino acids are listed herein below.
An amino acid to be added or substituted may be a non-natural amino acid.
A non-natural amino acid may have an atypical side chain.
The amino acid can be a natural or a non-natural amino acid.
Useful non-natural amino acids are described in the sections below.
Also polypeptides containing modified or non-natural amino acids are encompassed.
Exemplary non-natural amino acids are described in the sections below.
Each amino acid can be a natural or non-natural amino acid.
A non-natural amino acid denotes an analogue or derivative of a natural amino acid.
They may also comprise non-natural amino acids as indicated above.
See also
The non-natural amino acid polypeptide may be produced by ribosomal translation.
Substitutions may involve one or more natural or non-natural amino acids.
The non-natural amino acid may be linked to a water soluble polymer.
The numbers do not increase significantly if non-natural amino acids are included.
Any non-natural amino acid may be used in the present disclosure.
Another group of preferred modifications are non-natural amino acids and derivatives thereof.
The non-natural amino acid polypeptide may be produced in cell lysate.
Substitution or insertion may involve natural as well as non-natural amino acid residues.
A histidine or non-natural amino acid may be substituted or inserted at any site.
Also described herein are methods of making a polypeptide comprising a non-natural amino acid.
Any non-natural amino acid may be used in the present invention.
An amino acid residue can be a naturally-occurring or non-natural amino acid residue.
Any number of non-natural amino acids can be introduced into the polypeptide.
Alternatively, multiple sites may be substituted with histidine or non-natural amino acid.
It is possible to use non-natural amino acids known to those skilled in the art.
The amino acids described herein can be natural or non-natural amino acids.
The number of histidine or non-natural amino acid mutations is not particularly limited.
Non-natural amino acids also include amino acids having derivatized side groups.
The integer n represents the number of non-natural amino acids in the polypeptide chain.
The non-natural amino acid polypeptide may be produced by expression of the polynucleotide.
The amino acids used herein can also include non-natural amino acids.
In some embodiments, the non-natural amino acid is linked to a water soluble polymer.
Functional groups are specific groups of atoms within either natural or non-natural amino acids.
The non-natural amino acid can be synthetic or derived from another biological source.
Examples of peptide analogues include peptides comprising one or more non-natural amino acids.
In some embodiments, non-natural amino acids can be incorporated into the linker sequence.
Peptides according to the present embodiments may also contain non-natural amino acids.
Other similar approaches to obtain non-natural amino acids in a protein include methionine substitution methods.
The peptide molecule according to the present invention can comprise non-natural amino acids.
However, any naturally occurring and non-natural amino acids can be prepared by this method.
The non-natural amino acids are selected from amino acids having aromatic amine sidechains.
The extent of incorporation of the natural and non-natural amino acid may also vary.
Mesityl alanine is a non-natural amino acid useful for preparing several peptides and peptide analogs.
The generic term amino acid comprises both natural and non-natural amino acids.
In particular embodiments, any aromatic non-natural amino acid may be utilized with the modified PheRS.
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