The characteristics of purified HL60 tuftsin receptors |
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Authors: | Nancy J Bump Victor A Najjar Judith Reichler |
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Institution: | (1) Division of Protein Chemistry, Department of Molecular Biology and Microbiology, Tufts University School, of Medicine, Boston, Massachusetts, USA;(2) Dept. of Molecular Biology & Microbiology, Tufts University School of Medicine, 136 Harrison Avenue, 02111 Boston, MA, USA |
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Abstract: | Summary The purification and characteristics of purified HL60 tuftsin receptors are described. Purification was accomplished by affinity chromatography similar to that described earlier, wherein a tuftsin analog Thr-LysPro-Pro-Arg, is covalently linked at the N group to a solid support. The receptor consists presumably of two subunits approximately 66 KDa and 57 KDa. The dissociation constant of the receptor complex is 4.7 × 10–8 M with 5 × 104 receptors per cell. It can form oligomers with an Mr of about 560 KDa suggesting an octomeric structure, assuming the same number of each subunit is associated.Abbreviations CHAPS
3-(3-cholamidopropyl)dimethylammonio]-1-propanesulfonate
- DCC
Dicyclohexylcarbodiimide
- DMSO
Dimethylsulfoxide
- DSS
Disuccinimidylsuberate
- FCS
Fetal Calf Serum
- HEPES
4-(2-hydroxyethyl)-1-piperazineethanesulfonic Acid
- MMP
Macrophage/Monocyte and Polymorphonuclear granulocytes
- Mr
Relative Molecular mass
- NaDodSO4
Sodium Dodecyl Sulfate
- PEG
Polyethylene Glycol
- SP
Sucrose Phosphate buffer
- TFMS
Trifluoromethanesulfonic Acid |
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Keywords: | tuftsin receptors membrane protein |
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