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Inspiration from the mirror: D-amino acid containing peptides in biomedical approaches
- Source :
- Biomolecular Concepts, Vol 7, Iss 3, Pp 179-187 (2016)
- Publication Year :
- 2016
- Publisher :
- Walter de Gruyter GmbH, 2016.
-
Abstract
- D-amino acids, the enantiomers of naturally abundant L-amino acids, bear unique stereochemistry properties that lead to the resistance towards most of the endogenous enzymes. Previous works have demonstrated applications of D-amino acids in therapeutic development with the aid of mirror-image phage display and retro-inverso peptide synthesis. In this review, we highlight the recent progress and challenges in the exploration of D-amino acids at the interface of chemistry and life science. First, we will introduce some progress made in traditional application of D-amino acids to enhance biostability of peptide therapeutics. Then, we discuss some works that explore the relatively underexplored interactions between the enzyme and D-amino acids and enzymatic reactions of D-amino acids. To highlight the enzymatic reactions of D-amino acids, we will describe several emerging works on the enzyme-instructed self-assembly (EISA) and their potential application in selective anti-inflammatory or anticancer therapies. At the end, we briefly mention the challenges and possible future directions.
- Subjects :
- 0301 basic medicine
Phage display
QH301-705.5
Anti-Inflammatory Agents
Antineoplastic Agents
Peptide
010402 general chemistry
01 natural sciences
Article
General Biochemistry, Genetics and Molecular Biology
03 medical and health sciences
Cellular and Molecular Neuroscience
chemistry.chemical_compound
Peptide synthesis
Humans
D-amino acid
Amino Acids
biostability
Biology (General)
enzymatic reaction
chemistry.chemical_classification
anti-inflammatory and anticancer drugs
Stereoisomerism
General Medicine
0104 chemical sciences
Amino acid
030104 developmental biology
chemistry
Biochemistry
Endogenous enzymes
enzyme-instructed self-assembly
d-amino acids
Peptides
Subjects
Details
- ISSN :
- 1868503X and 18685021
- Volume :
- 7
- Database :
- OpenAIRE
- Journal :
- Biomolecular Concepts
- Accession number :
- edsair.doi.dedup.....4c15d5eb85834002ba018fb31669cd1b
- Full Text :
- https://doi.org/10.1515/bmc-2015-0035