The carbonic anhydrases : new horizons

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Bibliographic Information

The carbonic anhydrases : new horizons

edited by W.R. Chegwidden, N.D. Carter and Y.H. Edwards

(EXS, 90)

Birkhäuser Verlag, c2000

  • : sz

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Note

Includes bibliographical references and index

Description and Table of Contents

Volume

ISBN 9783764356705

Description

Carbonic anhydrase (CA) is a seemingly ubiquitous enzyme of profound physiological importance, which plays essential roles in respiration, acid-base homeostasis, bone resorption, calcification, photosynthesis, several biosynthetic pathways and a variety of processes involving ion, gas and fluid transfer. This enzyme, which is present in at least three gene families (a, ss, ?), has found favour as a model for the study of evolution of gene families and for site-directed mutagenesis in structure/function relationships, for protein folding and for transgenic and gene target studies. Since the early use of CA inhibitors as diuretics and in treating congestive heart failure, the enzyme has been target of considerable clinical attention. Much of this is now focused on endeavours to produce a new generation of such drugs for the effective treatment of glaucoma and other potential applications. Recent data, suggesting links between CA and various disease processes, including cancer, have stimulated further...

Table of Contents

Exordium: Remarks on the discovery of carbonic anhydrase.- to the carbonic anhydrases.- Evolution and distribution of the carbonic anhydrase gene families.- An overview of the distribution and function of carbonic anhydrase isozymes in mammals.- The membrane carbonic anhydrases: from CO2transport to tumour markers.- Carbonic anhydrase (CA)-related proteins (CA-RPs), and transmembrane proteins with CA or CA-RP domains.- Regulation of the CA 1, CA 2 and CA 3 genes.- Use of carbonic anhydrase II-deficient mice in uncovering the cellular location of membrane-associated isoforms.- X-ray crystallographic studies of mammalian carbonic anhydrase isozymes.- The catalytic mechanism of mammalian carbonic anhydrases.- Activation of carbonic anhydrase isozymes.- Active-site engineering of carbonic anhydrase and its application to biosensors.- Folding and stability of human carbonic anhydrase II.- Membrane transport and provision of substrates for carbonic anhydrase in vertebrates.- Respiratory and renal roles of carbonic anhydrase in gas exchange and acid-base regulation.- The roles of carbonic anhydrase in metabolism, cell growth and cancer in animals.- The roles of carbonic anhydrase in gustation, olefaction and chemical irritation.- Carbonic anhydrases in striated muscle.- Inherited deficiencies and activity variants of the mammalian carbonic anhydrases.- Carbonic anhydrase inhibition in ophthalmology: Carbonic anhydrase in cornea, lens, retina and lacrimal gland.- Carbonic anhydrase inhibition in ophthalmology: Aqueous humour secretion and development of sulphonamide inhibitors.- The design of new carbonic anhydrase inhibitors.- Roles of carbonic anhydrases in the alimentary tract.- Carbonic anhydrases in the nervous system.- Carbonic anhydrases in calcified tissues.- Carbonic anhydrases of higher plants: an overview.- Plant carbonic anhydrases: structure and mechanism.- Algal carbonic anhydrase.- Bacterial carbonic anhydrases.- Keeping pace with a fast enzyme: steps and missteps.- Carbonic anhydrase research: A clinical perspective, past and future.
Volume

: sz ISBN 9783764358518

Description

The chapters in this text are broadly organized so they trace the clinical course of the acute and chronic inflammatory response, emphasizing the therapeutic implications of data on the contribution of nitric oxide and related nitrogen-centred species.

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  • EXS

    Birkhäuser Verlag

Details

  • NCID
    BA52131151
  • ISBN
    • 3764358513
    • 3764356707
  • LCCN
    00027796
  • Country Code
    sz
  • Title Language Code
    eng
  • Text Language Code
    eng
  • Place of Publication
    Basel ; Boston
  • Pages/Volumes
    xviii, 619 p.
  • Size
    24 cm
  • Parent Bibliography ID
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