Radiation inactivation analysis of the A"1 adenosine receptor of rat brain Decrease in radiation inactivation size in the presence of guanine nucleotide
Radiation inactivation analysis of the binding of the A"1 adenosine receptor antagonist, 8-cyclopentyl-1,3-dipropylxanthine to rat brain membranes yielded a radiation inactivation size of 58 kDa. In the presence of GTPγS this was reduced to 33 kDa, in good agreement with the size of the ligand-...
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| Format: |
E-Artikel |
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| Sprache: |
Englisch |
| Erschienen: |
1989 |
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| Reproduktion: |
Elsevier Journal Backfiles on ScienceDirect 1907 - 2002 |
|---|---|
| Übergeordnetes Werk: |
in: FEBS Letters - Amsterdam : Elsevier, 252(1989), 1-2, Seite 125-128 |
| Übergeordnetes Werk: |
volume:252 ; year:1989 ; number:1-2 ; pages:125-128 |
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NLEJ173206271 |
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| 520 | |a Radiation inactivation analysis of the binding of the A"1 adenosine receptor antagonist, 8-cyclopentyl-1,3-dipropylxanthine to rat brain membranes yielded a radiation inactivation size of 58 kDa. In the presence of GTPγS this was reduced to 33 kDa, in good agreement with the size of the ligand-binding subunit detected after photoaffinity labelling. The data indicate that the structural association of A"1 adenosine receptors with G-protein components is altered in situ in the presence of guanine nucleotides. | ||
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(DE-627)NLEJ173206271 (DE-599)GBVNLZ173206271 DE-627 ger DE-627 rakwb eng Radiation inactivation analysis of the A"1 adenosine receptor of rat brain Decrease in radiation inactivation size in the presence of guanine nucleotide 1989 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Radiation inactivation analysis of the binding of the A"1 adenosine receptor antagonist, 8-cyclopentyl-1,3-dipropylxanthine to rat brain membranes yielded a radiation inactivation size of 58 kDa. In the presence of GTPγS this was reduced to 33 kDa, in good agreement with the size of the ligand-binding subunit detected after photoaffinity labelling. The data indicate that the structural association of A"1 adenosine receptors with G-protein components is altered in situ in the presence of guanine nucleotides. Elsevier Journal Backfiles on ScienceDirect 1907 - 2002 Reddington, M. oth Klotz, K.-N. oth Lohse, M.J. oth Hietel, B. oth in FEBS Letters Amsterdam : Elsevier 252(1989), 1-2, Seite 125-128 (DE-627)NLEJ173141048 (DE-600)1460391-3 0014-5793 nnns volume:252 year:1989 number:1-2 pages:125-128 http://linkinghub.elsevier.com/retrieve/pii/0014-5793(89)80903-2 GBV_USEFLAG_H ZDB-1-SDJ GBV_NL_ARTICLE AR 252 1989 1-2 125-128 |
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(DE-627)NLEJ173206271 (DE-599)GBVNLZ173206271 DE-627 ger DE-627 rakwb eng Radiation inactivation analysis of the A"1 adenosine receptor of rat brain Decrease in radiation inactivation size in the presence of guanine nucleotide 1989 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Radiation inactivation analysis of the binding of the A"1 adenosine receptor antagonist, 8-cyclopentyl-1,3-dipropylxanthine to rat brain membranes yielded a radiation inactivation size of 58 kDa. In the presence of GTPγS this was reduced to 33 kDa, in good agreement with the size of the ligand-binding subunit detected after photoaffinity labelling. The data indicate that the structural association of A"1 adenosine receptors with G-protein components is altered in situ in the presence of guanine nucleotides. Elsevier Journal Backfiles on ScienceDirect 1907 - 2002 Reddington, M. oth Klotz, K.-N. oth Lohse, M.J. oth Hietel, B. oth in FEBS Letters Amsterdam : Elsevier 252(1989), 1-2, Seite 125-128 (DE-627)NLEJ173141048 (DE-600)1460391-3 0014-5793 nnns volume:252 year:1989 number:1-2 pages:125-128 http://linkinghub.elsevier.com/retrieve/pii/0014-5793(89)80903-2 GBV_USEFLAG_H ZDB-1-SDJ GBV_NL_ARTICLE AR 252 1989 1-2 125-128 |
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(DE-627)NLEJ173206271 (DE-599)GBVNLZ173206271 DE-627 ger DE-627 rakwb eng Radiation inactivation analysis of the A"1 adenosine receptor of rat brain Decrease in radiation inactivation size in the presence of guanine nucleotide 1989 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Radiation inactivation analysis of the binding of the A"1 adenosine receptor antagonist, 8-cyclopentyl-1,3-dipropylxanthine to rat brain membranes yielded a radiation inactivation size of 58 kDa. In the presence of GTPγS this was reduced to 33 kDa, in good agreement with the size of the ligand-binding subunit detected after photoaffinity labelling. The data indicate that the structural association of A"1 adenosine receptors with G-protein components is altered in situ in the presence of guanine nucleotides. Elsevier Journal Backfiles on ScienceDirect 1907 - 2002 Reddington, M. oth Klotz, K.-N. oth Lohse, M.J. oth Hietel, B. oth in FEBS Letters Amsterdam : Elsevier 252(1989), 1-2, Seite 125-128 (DE-627)NLEJ173141048 (DE-600)1460391-3 0014-5793 nnns volume:252 year:1989 number:1-2 pages:125-128 http://linkinghub.elsevier.com/retrieve/pii/0014-5793(89)80903-2 GBV_USEFLAG_H ZDB-1-SDJ GBV_NL_ARTICLE AR 252 1989 1-2 125-128 |
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(DE-627)NLEJ173206271 (DE-599)GBVNLZ173206271 DE-627 ger DE-627 rakwb eng Radiation inactivation analysis of the A"1 adenosine receptor of rat brain Decrease in radiation inactivation size in the presence of guanine nucleotide 1989 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Radiation inactivation analysis of the binding of the A"1 adenosine receptor antagonist, 8-cyclopentyl-1,3-dipropylxanthine to rat brain membranes yielded a radiation inactivation size of 58 kDa. In the presence of GTPγS this was reduced to 33 kDa, in good agreement with the size of the ligand-binding subunit detected after photoaffinity labelling. The data indicate that the structural association of A"1 adenosine receptors with G-protein components is altered in situ in the presence of guanine nucleotides. Elsevier Journal Backfiles on ScienceDirect 1907 - 2002 Reddington, M. oth Klotz, K.-N. oth Lohse, M.J. oth Hietel, B. oth in FEBS Letters Amsterdam : Elsevier 252(1989), 1-2, Seite 125-128 (DE-627)NLEJ173141048 (DE-600)1460391-3 0014-5793 nnns volume:252 year:1989 number:1-2 pages:125-128 http://linkinghub.elsevier.com/retrieve/pii/0014-5793(89)80903-2 GBV_USEFLAG_H ZDB-1-SDJ GBV_NL_ARTICLE AR 252 1989 1-2 125-128 |
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(DE-627)NLEJ173206271 (DE-599)GBVNLZ173206271 DE-627 ger DE-627 rakwb eng Radiation inactivation analysis of the A"1 adenosine receptor of rat brain Decrease in radiation inactivation size in the presence of guanine nucleotide 1989 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Radiation inactivation analysis of the binding of the A"1 adenosine receptor antagonist, 8-cyclopentyl-1,3-dipropylxanthine to rat brain membranes yielded a radiation inactivation size of 58 kDa. In the presence of GTPγS this was reduced to 33 kDa, in good agreement with the size of the ligand-binding subunit detected after photoaffinity labelling. The data indicate that the structural association of A"1 adenosine receptors with G-protein components is altered in situ in the presence of guanine nucleotides. Elsevier Journal Backfiles on ScienceDirect 1907 - 2002 Reddington, M. oth Klotz, K.-N. oth Lohse, M.J. oth Hietel, B. oth in FEBS Letters Amsterdam : Elsevier 252(1989), 1-2, Seite 125-128 (DE-627)NLEJ173141048 (DE-600)1460391-3 0014-5793 nnns volume:252 year:1989 number:1-2 pages:125-128 http://linkinghub.elsevier.com/retrieve/pii/0014-5793(89)80903-2 GBV_USEFLAG_H ZDB-1-SDJ GBV_NL_ARTICLE AR 252 1989 1-2 125-128 |
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radiation inactivation analysis of the a"1 adenosine receptor of rat brain decrease in radiation inactivation size in the presence of guanine nucleotide |
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Radiation inactivation analysis of the A"1 adenosine receptor of rat brain Decrease in radiation inactivation size in the presence of guanine nucleotide |
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Radiation inactivation analysis of the binding of the A"1 adenosine receptor antagonist, 8-cyclopentyl-1,3-dipropylxanthine to rat brain membranes yielded a radiation inactivation size of 58 kDa. In the presence of GTPγS this was reduced to 33 kDa, in good agreement with the size of the ligand-binding subunit detected after photoaffinity labelling. The data indicate that the structural association of A"1 adenosine receptors with G-protein components is altered in situ in the presence of guanine nucleotides. |
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Radiation inactivation analysis of the binding of the A"1 adenosine receptor antagonist, 8-cyclopentyl-1,3-dipropylxanthine to rat brain membranes yielded a radiation inactivation size of 58 kDa. In the presence of GTPγS this was reduced to 33 kDa, in good agreement with the size of the ligand-binding subunit detected after photoaffinity labelling. The data indicate that the structural association of A"1 adenosine receptors with G-protein components is altered in situ in the presence of guanine nucleotides. |
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Radiation inactivation analysis of the binding of the A"1 adenosine receptor antagonist, 8-cyclopentyl-1,3-dipropylxanthine to rat brain membranes yielded a radiation inactivation size of 58 kDa. In the presence of GTPγS this was reduced to 33 kDa, in good agreement with the size of the ligand-binding subunit detected after photoaffinity labelling. The data indicate that the structural association of A"1 adenosine receptors with G-protein components is altered in situ in the presence of guanine nucleotides. |
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