Structural studies of the O-specific chain of Hafnia alvei strain PCM 1190 lipopolysaccharide

1997 ◽  
Vol 298 (3) ◽  
pp. 219-227 ◽  
Author(s):  
Carl Petersson ◽  
Wojciech Jachymek ◽  
Lennart Kenne ◽  
Tomasz Niedziela ◽  
Czeslaw Lugowski
1996 ◽  
Vol 292 ◽  
pp. 117-128 ◽  
Author(s):  
Wojciech Jachymek ◽  
Carl Petersson ◽  
Anne Helander ◽  
Lennart Kenne ◽  
Tomasz Niedziela ◽  
...  

1999 ◽  
Vol 266 (1) ◽  
pp. 53-61 ◽  
Author(s):  
Wojciech Jachymek ◽  
Jolanta Czaja ◽  
Tomasz Niedziela ◽  
Czeslaw Lugowski ◽  
Lennart Kenne

1997 ◽  
Vol 244 (2) ◽  
pp. 580-586 ◽  
Author(s):  
Carl Petersson ◽  
Tomasz Niedziela ◽  
Wojciech Jachymek ◽  
Lennart Kenne ◽  
Przemyslaw Zarzecki ◽  
...  

1995 ◽  
Vol 269 (1) ◽  
pp. 125-138 ◽  
Author(s):  
Wojciech Jachymek ◽  
Carl Petersson ◽  
Anne Helander ◽  
Lennart Kenne ◽  
Czeslaw Lugowski ◽  
...  

1996 ◽  
Vol 237 (3) ◽  
pp. 635-641 ◽  
Author(s):  
Tomasz Niedziela ◽  
Carl Petersson ◽  
Anne Helander ◽  
Wojciech Jachymek ◽  
Lennart Kenne ◽  
...  

1997 ◽  
Vol 245 (3) ◽  
pp. 668-675 ◽  
Author(s):  
Carl Petersson ◽  
Wojciech Jachymek ◽  
Agnieszka Klonowska ◽  
Czeslaw Lugowski ◽  
Tomasz Niedziela ◽  
...  

Author(s):  
James A. Lake

The understanding of ribosome structure has advanced considerably in the last several years. Biochemists have characterized the constituent proteins and rRNA's of ribosomes. Complete sequences have been determined for some ribosomal proteins and specific antibodies have been prepared against all E. coli small subunit proteins. In addition, a number of naturally occuring systems of three dimensional ribosome crystals which are suitable for structural studies have been observed in eukaryotes. Although the crystals are, in general, too small for X-ray diffraction, their size is ideal for electron microscopy.


Author(s):  
J.R. Mcintosh

The mitotic apparatus is a structure of obvious biological and medical interest, but it has proved to be a difficult cellular machine to understand. The chemical composition of the spindle is only slightly elucidated, largely because of the difficulties in preparing useful isolates of the structure. Chemical studies of the mitotic spindle have been reviewed elsewhere (Mcintosh, 1977), and will not be discussed further here. One would think that structural studies on the mitotic apparatus (MA) in situ would be straightforward, but even with this approach there is some disagreement in the results obtained with various methods and by different investigators. In this paper I will review briefly the approaches which have been used in structural studies of the MA, pointing out the strengths and problems of each approach. I will summarize the principal findings of the different methods, and identify what seem to be fruitful avenues for further work.


Author(s):  
A.M.H. Schepman ◽  
J.A.P. van der Voort ◽  
J.E. Mellema

A Scanning Transmission Electron Microscope (STEM) was coupled to a small computer. The system (see Fig. 1) has been built using a Philips EM400, equipped with a scanning attachment and a DEC PDP11/34 computer with 34K memory. The gun (Fig. 2) consists of a continuously renewed tip of radius 0.2 to 0.4 μm of a tungsten wire heated just below its melting point by a focussed laser beam (1). On-line operation procedures were developped aiming at the reduction of the amount of radiation of the specimen area of interest, while selecting the various imaging parameters and upon registration of the information content. Whereas the theoretical limiting spot size is 0.75 nm (2), routine resolution checks showed minimum distances in the order 1.2 to 1.5 nm between corresponding intensity maxima in successive scans. This value is sufficient for structural studies of regular biological material to test the performance of STEM over high resolution CTEM.


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