中国物理B ›› 2001, Vol. 10 ›› Issue (13): 100-107.

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IDENTIFICATION OF MEMBRANE PROTEINS IMAGED BY ATOMIC FORCE MICROSCOPY USING A TEMPLATE MATCHING ALGORITHM

Enrico Martinoia1, Oliver Enders2, Carsten Zeilinger2, Hans-Albert Kolb2   

  1. (1)Institut de Botanique, Laboratoire de Physiologie Végétale, Rue Emile-Argand 13, CH-2007 Neuchatel; (2)Institute of Biophysics, University of Hanover, Herrenh?user Str. 2, D-30419 Hannover
  • 收稿日期:2000-12-02 修回日期:2001-03-19 出版日期:2001-12-25 发布日期:2005-07-07

IDENTIFICATION OF MEMBRANE PROTEINS IMAGED BY ATOMIC FORCE MICROSCOPY USING A TEMPLATE MATCHING ALGORITHM

Oliver Endersa, Enrico Martinoiab, Carsten Zeilingera, Hans-Albert Kolba   

  1. a Institute of Biophysics, University of Hanover, Herrenh?user Str. 2, D-30419 Hannover; b Institut de Botanique, Laboratoire de Physiologie Végétale, Rue Emile-Argand 13, CH-2007 Neuchatel
  • Received:2000-12-02 Revised:2001-03-19 Online:2001-12-25 Published:2005-07-07

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摘要： The atomic force microscope allows to image biological samples in their native environment. But the identification and the topography of individual randomly distributed membrane proteins is still a challenge. We used membranes of isolated vacuoles of barley mesophyll cells. Images at low resolution indicate that vacuoles spontaneously attach, rupture and finally adsorb completely as planar membrane to mica. Height profiles indicate that the membrane at the peripheral boundary exposes the extravacuolar surface to the scanning tip. At molecular resolution a template matching correlation algorithm was used to identify the most abundant membrane protein, the vacuolar H+-ATPase by the characteristic extravacuolar head of the transport molecule. The data indicate the possibility to analyse single randomly distributed membrane proteins in their native environment with the knowledge of a suitable template.

Abstract: The atomic force microscope allows to image biological samples in their native environment. But the identification and the topography of individual randomly distributed membrane proteins is still a challenge. We used membranes of isolated vacuoles of barley mesophyll cells. Images at low resolution indicate that vacuoles spontaneously attach, rupture and finally adsorb completely as planar membrane to mica. Height profiles indicate that the membrane at the peripheral boundary exposes the extravacuolar surface to the scanning tip. At molecular resolution a template matching correlation algorithm was used to identify the most abundant membrane protein, the vacuolar H+-ATPase by the characteristic extravacuolar head of the transport molecule. The data indicate the possibility to analyse single randomly distributed membrane proteins in their native environment with the knowledge of a suitable template.

Key words: atomic force microscope, vacuolar membrane, H+-ATPase, template matching

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