| Autor: |
Raman, Dayanidhi, Neel, Nicole F., Sai, Jiqing, Mernaugh, Raymond L., Ham, Amy-Joan L., Richmond, Ann J. |
| Zdroj: |
Methods in Enzymology; 2009, Vol. 460, p315-330, 16p |
| Abstrakt: |
Abstract: Chemokine‐receptor signaling is initiated upon ligand binding to the receptor and continues through the process of endocytic trafficking by the association of a variety of adaptor proteins with the chemokine receptor. In order to define the adaptor proteins that associate with CXCR2 before and after ligand activation, a protocol was developed using differentiated HL‐60 cells transfected to express CXCR2 stimulated or not stimulated with ligand for one minute. CXCR2‐associating proteins were isolated by immunoprecipitation with CXCR2 antibody and the eluted proteins were electrophoretically run into the separating gel directly without a stacking gel. The stained single band was subjected to in-gel trypsin digestion. The tryptic peptides were subjected to, LC/MS/MS proteomic analysis. Proteins identified in a minimum of three of four separate experiments with multiple peptides were then validated as CXCR2 adaptor proteins by coimmunoprecipitation, GST pull‐down studies, and immunocytochemical CXCR2‐colocalization experiments using dHL‐60‐CXCR2 cells. Subsequently, a functional analysis of the interaction between CXCR2 and CXCR2 interacting proteins was performed. This approach can be used to characterize chemokine receptor–associating proteins over time both before and after ligand stimulation, allowing definition of the dynamic spatial and temporal formation of a “chemosynapse.” [Copyright &y& Elsevier] |
| Databáze: |
Supplemental Index |
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