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Isolation of leptin-binding peptides from a random peptide phage library.
- Source :
-
The journal of peptide research : official journal of the American Peptide Society [J Pept Res] 2000 Apr; Vol. 55 (4), pp. 318-24. - Publication Year :
- 2000
-
Abstract
- Leptin plays a role in regulating the body weight in mice. Injection of recombinant mouse leptin expressed in Escherichia coli reduced the food intake and body weight in normal, ob/ob and diet-induced obesity mice. Hyperglycemia, hyperinsulinemia and hypothermia can also be corrected in ob/ob mice after leptin injection. Leptin is a 16-kDa secretory protein comprising 167 amino acids produced in adipose tissue and is secreted to blood stream. In this study, a recombinant mouse leptin was generated and purified from a baculovirus expression system. This protein was used to identify putative ligands using a phage library of random peptides. Three leptin-binding phage clones were found, which were characterized by DNA sequencing and ELISA methods. The amino acid sequences of the reactive peptides are: LAYCSDPVRCLVWWY, MFWISAVSFVDHALV and LVLVLSAFLCCGVG. All three clones bound to recombinant human and mouse leptins. These peptides may be useful tools to study leptin-receptor interaction, food intake and body weight regulation.
- Subjects :
- Amino Acid Sequence
Animals
Bacteriophages metabolism
Baculoviridae genetics
Base Sequence
Cell Line
Enzyme-Linked Immunosorbent Assay
Escherichia coli genetics
Escherichia coli metabolism
Genetic Vectors
Humans
Insecta cytology
Leptin chemistry
Leptin genetics
Ligands
Mice
Molecular Sequence Data
Peptide Library
Peptides genetics
Peptides isolation & purification
Protein Binding
Recombinant Proteins genetics
Recombinant Proteins isolation & purification
Recombinant Proteins metabolism
Sequence Analysis, DNA
Leptin metabolism
Peptides metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1397-002X
- Volume :
- 55
- Issue :
- 4
- Database :
- MEDLINE
- Journal :
- The journal of peptide research : official journal of the American Peptide Society
- Publication Type :
- Academic Journal
- Accession number :
- 10798377
- Full Text :
- https://doi.org/10.1034/j.1399-3011.2000.00679.x