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Visualizing Intramolecular Dynamics of Membrane Proteins.

Tatsunari OhkuboTakaaki ShiinaKayoko KawaguchiDaisuke SasakiRena InamasuYue YangZhuoqi LiKeizaburo TaninakaMasaki SakaguchiShoko FujimuraHiroshi SekiguchiMasahiro KuramochiTatsuya AraiSakae TsudaYuji C SasakiKazuhiro Mio
Published in: International journal of molecular sciences (2022)
Membrane proteins play important roles in biological functions, with accompanying allosteric structure changes. Understanding intramolecular dynamics helps elucidate catalytic mechanisms and develop new drugs. In contrast to the various technologies for structural analysis, methods for analyzing intramolecular dynamics are limited. Single-molecule measurements using optical microscopy have been widely used for kinetic analysis. Recently, improvements in detectors and image analysis technology have made it possible to use single-molecule determination methods using X-rays and electron beams, such as diffracted X-ray tracking (DXT), X-ray free electron laser (XFEL) imaging, and cryo-electron microscopy (cryo-EM). High-speed atomic force microscopy (HS-AFM) is a scanning probe microscope that can capture the structural dynamics of biomolecules in real time at the single-molecule level. Time-resolved techniques also facilitate an understanding of real-time intramolecular processes during chemical reactions. In this review, recent advances in membrane protein dynamics visualization techniques were presented.
Keyphrases
  • single molecule
  • atomic force microscopy
  • electron microscopy
  • high speed
  • high resolution
  • living cells
  • magnetic resonance
  • energy transfer
  • mass spectrometry
  • photodynamic therapy