4.5 Article

Subunit analysis of bovine heart complex I by reversed-phase high-performance liquid chromatography, electrospray ionization-tandem mass spectrometry, and matrix-assisted laser desorption/ionization-time-of-flight mass spectrometry

Journal

ANALYTICAL BIOCHEMISTRY
Volume 382, Issue 2, Pages 116-121

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.ab.2008.07.029

Keywords

NADH dehydrogenase; subunit analysis; mitochondrial electron transport complexes; liquid chromatography; MALDI-TOF; ESI/MS/MS

Funding

  1. National Institutes of Health [GMS 24795]
  2. Robert A. Welch Foundation [AQ1481]
  3. University of Texas Health Science Center, San Antonio [VPN 125644]

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An effective method was developed for isolation and analysis of bovine heart complex I subunits. The method Uses C18 reversed-phase high-performance liquid chromatography (HPLC) and a water/acetonitrile gradient containing 0.1% trifluoroacetic acid. Employing this system, 36 of the 45 complex I subunits elute in 28 distinct chromatographic peaks. The 9 subunits that do not elute are B14.7, MLRQ, and the 7 mitochondrial-encoded subunits. The method, With ultraviolet (UV) detection, is Suitable for either analytical (<50 mu g protein) or preparative (>250 mu g protein) applications. Subunits eluting in each chromatographic peak were initially determined by matrix-assisted laser desorption/ionization-time-of-flight/mass spectrometry (MALDI-TOF/MS) with subsequent positive identification by reversed-phase HPLC-electrospray ionization (ESI)/tandem mass spectrometry (MS/MS) analysis of tryptic digests. In the latter case, subunits were identified with a 99% probability using, Mascot for database searching and Scaffold for assessment of protein identification probabilities. The reversed-phase HPLC Subunit analysis. method represents a major improvement over previous separation methods with respect to resolution, simplicity, and ease of application. (C) 2008 Elsevier Inc. All rights reserved.

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