Literature DB >> 10497174

Electrospray ionization mass spectrometric determination of the molecular mass of the approximately 200-kDa globin dodecamer subassemblies in hexagonal bilayer hemoglobins.

B N Green1, R S Bordoli, L G Hanin, F H Lallier, A Toulmond, S N Vinogradov.   

Abstract

Hexagonal bilayer hemoglobins (Hbs) are approximately 3.6-MDa complexes of approximately 17-kDa globin chains and 24-32-kDa, nonglobin linker chains in a approximately 2:1 mass ratio found in annelids and related species. Studies of the dissociation and reassembly of Lumbricus terrestris Hb have provided ample evidence for the presence of a approximately 200-kDa linker-free subassembly consisting of monomer (M) and disulfide-bonded trimer (T) subunits. Electrospray ionization mass spectrometry (ESI-MS) of the subassemblies obtained by gel filtration of partially dissociated L. terrestris and Arenicola marina Hbs showed the presence of noncovalent complexes of M and T subunits with masses in the 213. 3-215.4 and 204.6-205.6 kDa ranges, respectively. The observed mass of the L. terrestris subassembly decreased linearly with an increase in de-clustering voltage from approximately 215,400 Da at 60 V to approximately 213,300 Da at 200 V. In contrast, the mass of the A. marina complex decreased linearly from 60 to 120 V and reached an asymptote at approximately 204,600 Da (180-200 V). The decrease in mass was probably due to the progressive removal of complexed water and alkali metal cations. ESI-MS at an acidic pH showed both subassemblies to consist of only M and T subunits, and the experimental masses demonstrated them to have the composition M(3)T(3). Because there are three isoforms of M and four isoforms of T in Lumbricus and two isoforms of M and 5 isoforms of T in Arenicola, the masses of the M(3)T(3) subassemblies are not unique. A random assembly model was used to calculate the mass distributions of the subassemblies, using the known ESI-MS masses and relative intensities of the M and T subunit isforms. The expected mass of randomly assembled subassemblies was 213,436 Da for Lumbricus Hb and 204,342 Da for Arenicola Hb, in good agreement with the experimental values.

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Year:  1999        PMID: 10497174     DOI: 10.1074/jbc.274.40.28206

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  8 in total

1.  Detection of intact megaDalton protein assemblies of vanillyl-alcohol oxidase by mass spectrometry.

Authors:  W J van Berkel; R H van den Heuvel; C Versluis; A J Heck
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2.  An electrospray ionization mass spectrometric study of the subunit structure of the giant hemoglobin from the leech Nephelopsis oscura.

Authors:  Brian N Green; Serge N Vinogradov
Journal:  J Am Soc Mass Spectrom       Date:  2004-01       Impact factor: 3.109

3.  Hemoglobin Porto Alegre forms a tetramer of tetramers superstructure.

Authors:  Véronique Baudin-Creuza; Christophe Fablet; Franck Zal; Brian N Green; Danielle Promé; Michael C Marden; Josée Pagnier; Henri Wajcman
Journal:  Protein Sci       Date:  2002-01       Impact factor: 6.725

4.  Real-time measurement of myosin-nucleotide noncovalent complexes by electrospray ionization mass spectrometry.

Authors:  Howard D White; Alison E Ashcroft
Journal:  Biophys J       Date:  2007-05-04       Impact factor: 4.033

5.  Globin and linker sequences of the giant extracellular hemoglobin from the leech Macrobdella decora.

Authors:  Tomohiko Suzuki; Serge N Vinogradov
Journal:  J Protein Chem       Date:  2003-04

6.  Comparative ESI-MS study of approximately 2.2 MDa native hemocyanins from deep-sea and shore crabs: from protein oligomeric state to biotope.

Authors:  Sarah Sanglier; Emmanuelle Leize; Alain Van Dorsselaer; Franck Zal
Journal:  J Am Soc Mass Spectrom       Date:  2003-05       Impact factor: 3.109

7.  Correct charge state assignment of native electrospray spectra of protein complexes.

Authors:  Lars Liepold; Luke M Oltrogge; Peter A Suci; Mark J Young; Trevor Douglas
Journal:  J Am Soc Mass Spectrom       Date:  2008-11-17       Impact factor: 3.109

8.  Metastable ion formation and disparate charge separation in the gas-phase dissection of protein assemblies studied by orthogonal time-of-flight mass spectrometry.

Authors:  C Versluis; A van der Staaij; E Stokvis; A J Heck; B de Craene
Journal:  J Am Soc Mass Spectrom       Date:  2001-03       Impact factor: 3.262

  8 in total

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