Literature DB >> 21789486

The analytical determination of isoprenoid intermediates from the mevalonate pathway.

Gudrun Nürenberg1, Dietrich A Volmer.   

Abstract

In this article, assays on the analytical determination of farnesyl pyrophosphate (FPP) and geranylgeranyl pyrophosphate (GGPP), two important isoprenoid intermediates at biochemically relevant branching points in the mevalonate pathway, are summarized and reviewed. There is considerable recent interest in the measurement of these two isoprenoids because of their direct involvement in several diseases, for example, statins lower cholesterol by inhibiting 3-hydroxy-3-methylglutaryl-CoA reductase but equally affect other metabolite biosyntheses. The isoprenoids FPP and GGPP are key intermediates due to their role as CaaX-specific substrates for posttranslational modification of proteins (protein prenylation). Disease pathologies and therapeutic efficacy of different treatments (e.g., cholesterol-lowering drugs) may lead to a reduction in isoprenoid levels and an accompanying reduction in prenylation of specific proteins. To understand the exact biochemical role of the isoprenoids FPP and GGPP, we need to know their levels. Several recent studies have shown exact levels of FPP and GGP in plasma and relevant tissues and their modulation following treatment. Furthermore, by directly measuring the extent of protein prenylation and identifying target proteins, further insight into the exact biochemical nature of the pathology and regulatory mechanisms will be possible. This short review aims to highlight the relevant literature on the analytical determination of the free isoprenoids FPP and GGPP in biological tissue as well as techniques for directly measuring prenylated proteins.

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Year:  2011        PMID: 21789486     DOI: 10.1007/s00216-011-5262-2

Source DB:  PubMed          Journal:  Anal Bioanal Chem        ISSN: 1618-2642            Impact factor:   4.142


  7 in total

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2.  Inhibition of endocytic lipid antigen presentation by common lipophilic environmental pollutants.

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Authors:  Ashley K Boyle; Sara F Rinaldi; Adriano G Rossi; Philippa T K Saunders; Jane E Norman
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4.  Lovastatin, not Simvastatin, Corrects Core Phenotypes in the Fragile X Mouse Model.

Authors:  Melania Muscas; Susana R Louros; Emily K Osterweil
Journal:  eNeuro       Date:  2019-06-12

5.  Simvastatin Inhibits Brucella abortus Invasion into RAW 264.7 Cells through Suppression of the Mevalonate Pathway and Promotes Host Immunity during Infection in a Mouse Model.

Authors:  Trang Thi Nguyen; Heejin Kim; Tran Xuan Ngoc Huy; Wongi Min; Hujang Lee; Alisha Wehdnesday Bernardo Reyes; Johnhwa Lee; Suk Kim
Journal:  Int J Mol Sci       Date:  2022-07-28       Impact factor: 6.208

6.  Transcriptome exploration of the sex pheromone gland of Lutzomyia longipalpis (Diptera: Psychodidae: Phlebotominae).

Authors:  Natalia González-Caballero; Jesus G Valenzuela; José M C Ribeiro; Patricia Cuervo; Reginaldo P Brazil
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7.  A Differential Effect of Lovastatin versus Simvastatin in Neurodevelopmental Disorders.

Authors:  Melania Muscas; Sang S Seo; Susana R Louros; Emily K Osterweil
Journal:  eNeuro       Date:  2020-08-13
  7 in total

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