Literature DB >> 6090217

Determination of the functional molecular size of vasopressin isoreceptors.

P Crause, R Boer, F Fahrenholz.   

Abstract

The molecular size of vasopressin receptors in the intact membrane-bound state was determined by radiation inactivation (target size analysis). For the V1 receptor in rat liver a molecular size of (76 +/- 8) kDa was determined. For the V2 receptor in rat kidney and bovine kidney molecular sizes of (95 +/- 4) and (108 +/- 11) kDa were found. Statistical analysis gave evidence for size differences between rat liver and rat kidney receptors or differences between rat liver and bovine kidney receptors, but not between kidney receptors from different species. The results suggest that V1 and V2 receptors can be distinguished by functional properties as well as by their size.

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Year:  1984        PMID: 6090217     DOI: 10.1016/0014-5793(84)80773-5

Source DB:  PubMed          Journal:  FEBS Lett        ISSN: 0014-5793            Impact factor:   4.124


  2 in total

1.  Vasopressin receptor subtypes: autoradiographic localization of V1 vasopressin binding sites in rat brain and kidney.

Authors:  F Fahrenholz; R Gerstberger
Journal:  J Protein Chem       Date:  1989-06

2.  Activation of V1-receptors by vasopressin stimulates inositol phospholipid hydrolysis and arachidonate metabolism in human platelets.

Authors:  W Siess; M Stifel; H Binder; P C Weber
Journal:  Biochem J       Date:  1986-01-01       Impact factor: 3.857

  2 in total

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