Isomerization kinetics of AT hook decapeptide solution structures

Anal Chem. 2014 Jan 21;86(2):1210-4. doi: 10.1021/ac403386q. Epub 2014 Jan 8.

Abstract

The mammalian high mobility group protein HMGA2 contains three DNA binding motifs associated with many physiological functions including oncogenesis, obesity, stem cell youth, human height, and human intelligence. In the present paper, trapped ion mobility spectrometry-mass spectrometry (TIMS-MS) has been utilized to study the conformational dynamics of the third DNA binding motif using the "AT hook" decapeptide unit (Lys(1)-Arg(2)-Prol(3)-Arg(4)-Gly(5)-Arg(6)-Prol(7)-Arg(8)-Lys(9)-Trp(10), ATHP) as a function of the solvent state. Solvent state distributions were preserved during electrospray ion formation, and multiple IMS bands were identified for the [M + 2H](2+) and for the [M + 3H](3+) charge states. Conformational isomer interconversion rates were measured as a function of the trapping time for the [M + 2H](2+) and [M + 3H](3+) charge states. Candidate structures were proposed for all IMS bands observed. Protonation site, proline residue conformation, and side chain orientations were identified as the main motifs governing the conformational interconversion processes. Conformational dynamics from the solvent state distribution to the gas-phase "de-solvated" state distribution demonstrated that ATHP is "structured", and relative abundances are associated with the relative stability between the proposed conformers. The most stable ATHP [M + 2H](2+) conformation at the "de-solvated" state corresponds to the AT hook motif observed in AT-rich DNA regions.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • AT-Hook Motifs
  • DNA / chemistry
  • HMGA2 Protein / chemistry*
  • Humans
  • Isomerism
  • Molecular Dynamics Simulation
  • Oligopeptides / chemistry*
  • Proline / chemistry
  • Protein Conformation
  • Protons*
  • Solutions
  • Spectrometry, Mass, Electrospray Ionization
  • Static Electricity

Substances

  • HMGA2 Protein
  • Oligopeptides
  • Protons
  • Solutions
  • DNA
  • Proline