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D1 cap region involved in the receptor recognition and neural cell survival activity of human ciliary neurotrophic factor
- Source :
- Proceedings of the National Academy of Sciences. 92:8579-8583
- Publication Year :
- 1995
- Publisher :
- Proceedings of the National Academy of Sciences, 1995.
-
Abstract
- Human ciliary neurotrophic factor (hCNTF), which promotes the cell survival and differentiation of motor and other neurons, is a protein belonging structurally to the alpha-helical cytokine family. hCNTF was subjected to three-dimensional structure modeling and site-directed mutagenesis to analyze its structure-function relationship. The replacement of Lys-155 with any other amino acid residue resulted in abolishment of neural cell survival activity, and some of the Glu-153 mutant proteins had 5- to 10-fold higher biological activity. The D1 cap region (around the boundary between the CD loop and helix D) of hCNTF, including both Glu-153 and Lys-155, was shown to play a key role in the biological activity of hCNTF as one of the putative receptor-recognition sites. In this article, the D1 cap region of the 4-helix-bundle proteins is proposed to be important in receptor recognition and biological activity common to alpha-helical cytokine proteins reactive with gp130, a component protein of the receptors.
- Subjects :
- Models, Molecular
Cell Survival
DNA Mutational Analysis
Molecular Sequence Data
Mutagenesis (molecular biology technique)
Nerve Tissue Proteins
Biology
Ciliary neurotrophic factor
Structure-Activity Relationship
Ganglia, Spinal
Humans
Structure–activity relationship
Ciliary Neurotrophic Factor
Nerve Growth Factors
Amino Acids
Receptor
Neurons
chemistry.chemical_classification
Multidisciplinary
Base Sequence
Dose-Response Relationship, Drug
Biological activity
Glycoprotein 130
Molecular biology
Protein Structure, Tertiary
Amino acid
Nerve growth factor
chemistry
Mutagenesis, Site-Directed
biology.protein
Cytokines
Research Article
Subjects
Details
- ISSN :
- 10916490 and 00278424
- Volume :
- 92
- Database :
- OpenAIRE
- Journal :
- Proceedings of the National Academy of Sciences
- Accession number :
- edsair.doi.dedup.....a343c609e1cf2837323640e05e8c885e
- Full Text :
- https://doi.org/10.1073/pnas.92.19.8579