Biochemical Characterization of β2-Adrenergic Receptor Dimers and Oligomers
| LEADER | caa a22 4500 | ||
|---|---|---|---|
| 001 | 378849522 | ||
| 003 | CHVBK | ||
| 005 | 20180305123320.0 | ||
| 007 | cr unu---uuuuu | ||
| 008 | 161128e20030127xx s 000 0 eng | ||
| 024 | 7 | 0 | |a 10.1515/BC.2003.012 |2 doi |
| 035 | |a (NATIONALLICENCE)gruyter-10.1515/BC.2003.012 | ||
| 245 | 0 | 0 | |a Biochemical Characterization of β2-Adrenergic Receptor Dimers and Oligomers |h [Elektronische Daten] |c [A. Salahpour, H. Bonin, S. Bhalla, U. Petäjä-Repo, M. Bouvier] |
| 520 | 3 | |a G Protein-coupled receptor dimerization/oligomerization has been well established during the last several years. Studies have demonstrated the existence of dimers/digomers both in vitro and in living cells. However, a thorough characterization of the biochemical nature of receptor dimers and oligomers as well as their occurrence at the cell surface has not been properly addressed. In this study, we show that both β2-adrenergic receptor (β2AR) dimers and oligomers exist at the plasma membrane and that the detection of such species, following receptor solubilization and resolution by denaturing polyacrylamide gel electrophoresis (SDS-PAGE), does not result from the formation of spurious disulfide bonds during cell lysis. Moreover, our results indicate that the biochemical nature of β2AR dimers is different from that of the oligomers. Although both complexes are partially resistant to SDS denaturation, disulfide bonding is absolutely required for the stability of β2AR oligomers but not dimers in SDS-PAGE. Indeed, dimeric species can be detected even in the presence of high concentrations of reducing and alkylating agents. Although the different biochemical nature of the dimers and oligomers may be indicative of distinct biological roles in cells, additional studies will be required to further elucidate the biosynthesis and function of these receptor forms. | |
| 540 | |a Copyright © 2003 by Walter de Gruyter GmbH & Co. KG | ||
| 690 | 7 | |a Biochemistry |2 nationallicence | |
| 690 | 7 | |a Molecular biology |2 nationallicence | |
| 690 | 7 | |a Cellular biology |2 nationallicence | |
| 700 | 1 | |a Salahpour |D A. |4 aut | |
| 700 | 1 | |a Bonin |D H. |4 aut | |
| 700 | 1 | |a Bhalla |D S. |4 aut | |
| 700 | 1 | |a Petäjä-Repo |D U. |4 aut | |
| 700 | 1 | |a Bouvier |D M. |4 aut | |
| 773 | 0 | |t Biological Chemistry |d Walter de Gruyter |g 384/1(2003-01-27), 117-123 |x 1431-6730 |q 384:1<117 |1 2003 |2 384 |o bchm | |
| 856 | 4 | 0 | |u https://doi.org/10.1515/BC.2003.012 |q text/html |z Onlinezugriff via DOI |
| 908 | |D 1 |a research article |2 jats | ||
| 950 | |B NATIONALLICENCE |P 856 |E 40 |u https://doi.org/10.1515/BC.2003.012 |q text/html |z Onlinezugriff via DOI | ||
| 950 | |B NATIONALLICENCE |P 700 |E 1- |a Salahpour |D A. |4 aut | ||
| 950 | |B NATIONALLICENCE |P 700 |E 1- |a Bonin |D H. |4 aut | ||
| 950 | |B NATIONALLICENCE |P 700 |E 1- |a Bhalla |D S. |4 aut | ||
| 950 | |B NATIONALLICENCE |P 700 |E 1- |a Petäjä-Repo |D U. |4 aut | ||
| 950 | |B NATIONALLICENCE |P 700 |E 1- |a Bouvier |D M. |4 aut | ||
| 950 | |B NATIONALLICENCE |P 773 |E 0- |t Biological Chemistry |d Walter de Gruyter |g 384/1(2003-01-27), 117-123 |x 1431-6730 |q 384:1<117 |1 2003 |2 384 |o bchm | ||
| 900 | 7 | |b CC0 |u http://creativecommons.org/publicdomain/zero/1.0 |2 nationallicence | |
| 898 | |a BK010053 |b XK010053 |c XK010000 | ||
| 949 | |B NATIONALLICENCE |F NATIONALLICENCE |b NL-gruyter | ||