Tonks, N. K., Diltz, C. D., Fischer, E. H. (1991) Purification and assay of CD45: an integral membrane protein-tyrosine phosphatase. Methods in Enzymology, 201. pp. 442-451. ISSN 0076-6879
Abstract
This chapter discusses purification and assay of CD45 of an integral membrane protein-tyrosine phosphatase. The determination of the amino acid sequence of protein-tyrosine phosphatase (PTPase) 1B, a major low-molecular-weight PTPase isolated from human placenta, has demonstrated that this enzyme is not structurally related to the protein-Ser/Thr phosphatases. CD45 represents a family of high-molecular-weight (180k–220k) integral membrane proteins, the expression of which is restricted to cells of the hematopoietic lineage. The molecule can be defined in terms of three segments. The intracellular segment is highly conserved between isoforms and comprises two homologous domains of ∼300 residues, each structurally equivalent to one PTPase molecule. The intracellular and extracellular segments are connected by a single transmembrane hydrophobic stretch of 22 residues. A simple procedure for the purification and assay of CD45 is described in the chapter.
| Item Type: | Paper |
|---|---|
| Uncontrolled Keywords: | HUMAN-PLACENTA FAMILY KINASE |
| Subjects: | bioinformatics > genomics and proteomics > genetics & nucleic acid processing > protein structure, function, modification > protein types > enzymes bioinformatics > genomics and proteomics > genetics & nucleic acid processing > protein structure, function, modification > protein types bioinformatics > genomics and proteomics > genetics & nucleic acid processing > protein structure, function, modification > protein types > enzymes > protein tyrosine phosphatase |
| CSHL Authors: | |
| Communities: | CSHL labs > Tonks lab |
| Depositing User: | Matt Covey |
| Date: | 1991 |
| Date Deposited: | 17 Dec 2013 15:30 |
| Last Modified: | 17 Dec 2013 15:30 |
| Related URLs: | |
| URI: | https://repository.cshl.edu/id/eprint/29088 |
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