Literature DB >> 1413253

In situ investigations of single living cells infected by viruses.

W Häberle1, J K Hörber, F Ohnesorge, D P Smith, G Binnig.   

Abstract

In this paper we report the direct observation of biological processes on living cells. The experiments were done in situ by scanning force microscopy on a scale inaccessible by other techniques under physiological conditions. Living monkey-kidney cultured cells were imaged under normal growth conditions and showed reproducible features on the 10 nm scale. Upon adding a suspension of pox viruses, characteristic changes of the cell membrane were repeatedly observed in different experiments on different cells. Almost immediately, a pronounced softening of the cell surface occurred which lasted only for a few minutes. More than two hours later very significant protrusions appeared to grow out of the cell membrane. These protrusions abruptly disappeared again. These events were only observed after infection and we interpret them as the exocytosis of proteins related to viral reproduction. After almost 20 h, a different type of event occurred which we interpret as the exocytosis of the progeny viruses themselves.

Mesh:

Year:  1992        PMID: 1413253     DOI: 10.1016/0304-3991(92)90418-j

Source DB:  PubMed          Journal:  Ultramicroscopy        ISSN: 0304-3991            Impact factor:   2.689


  21 in total

Review 1.  Sampling protein form and function with the atomic force microscope.

Authors:  Marian Baclayon; Wouter H Roos; Gijs J L Wuite
Journal:  Mol Cell Proteomics       Date:  2010-06-18       Impact factor: 5.911

2.  Directly monitoring individual retrovirus budding events using atomic force microscopy.

Authors:  Micha Gladnikoff; Itay Rousso
Journal:  Biophys J       Date:  2007-09-07       Impact factor: 4.033

Review 3.  AFM review study on pox viruses and living cells.

Authors:  F M Ohnesorge; J K Hörber; W Häberle; C P Czerny; D P Smith; G Binnig
Journal:  Biophys J       Date:  1997-10       Impact factor: 4.033

4.  Direct observation of protein secondary structure in gas vesicles by atomic force microscopy.

Authors:  T J McMaster; M J Miles; A E Walsby
Journal:  Biophys J       Date:  1996-05       Impact factor: 4.033

5.  Cell viability and probe-cell membrane interactions of XR1 glial cells imaged by atomic force microscopy.

Authors:  S S Schaus; E R Henderson
Journal:  Biophys J       Date:  1997-09       Impact factor: 4.033

Review 6.  High-speed atomic force microscopy and its future prospects.

Authors:  Toshio Ando
Journal:  Biophys Rev       Date:  2017-12-18

7.  Atomic force microscopy studies of solid lipid nanoparticles.

Authors:  A zur Mühlen; E zur Mühlen; H Niehus; W Mehnert
Journal:  Pharm Res       Date:  1996-09       Impact factor: 4.200

8.  Atomic force microscopy of the myosin molecule.

Authors:  P Hallett; G Offer; M J Miles
Journal:  Biophys J       Date:  1995-04       Impact factor: 4.033

9.  Observation of living cells using the atomic force microscope.

Authors:  S Kasas; V Gotzos; M R Celio
Journal:  Biophys J       Date:  1993-02       Impact factor: 4.033

10.  Preparation of isolated biomolecules for SFM observations: T4 bacteriophage as a test sample.

Authors:  E Droz; M Taborelli; T N Wells; P Descouts
Journal:  Biophys J       Date:  1993-09       Impact factor: 4.033

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