Growth of cultured cells from patients with Fanconi anemia.

Fibroblast cultures derived from skin biopsies of patients with Fanconi anemia had doubling times (mean of five lines: 30.3 +/- 0.2 hours) significantly longer than randomly selected normal controls (mean of nine lines: 22.9 +/- 0.4 hours). Control cultures grew more slowly in the enriched media RPMI 1640 and McCoy's 5A than in MEM; while a culture from a patient with Fanconi anemia grew more slowly only in McCoy's 5A. Differences in growth characteristics between Fanconi anemia and normal cell cultures may be useful in analyzing the metabolic error determined by the Fanconi anemia gene.     

Inclusions within lipid droplets in some plant seeds

Summary Inclusions have been found within lipid droplets in cells of a number of air-dry seeds when investigated by freeze-etching. The inclusions invariably appear as depressions in the replicas. It is deduced that the inclusions are gaseous, and evidence from artificial preparations supports this.     

Marker-free method for accurate alignment between correlated light,cryo-light,and electron cryo-microscopy data using sample support features

Combining fluorescence microscopy with electron cryo-tomography allows, in principle, spatial localization of tagged macromolecular assemblies and structural features within the cellular environment. To allow precise localization and scale integration between the two disparate imaging modalities, accurate alignment procedures are needed. Here, we describe a marker-free method for aligning images from light or cryo-light fluorescence microscopy and from electron cryo-microscopy that takes advantage of sample support features, namely the holes in the carbon film. We find that the accuracy of this method, as judged by prediction errors of the hole center coordinates, is better than 100?nm.     

Carbon-13 nmr spectra of vitamin B6 compounds: Aqueous solution equilibria and determination of microscopic acid dissociation constants

The aqueous solution equilibria and solute structure of vitamin B₆ compounds and several model compounds have been investigated using ¹³C-nmr spectroscopy. The unsubstituted α-carbon of these compounds is a very good probe for data which permits assignment of the ionization steps to indicidual groups. While the ionizations of the pyridinium and phenolic groups take place simultaneously in 3-hydroxypyridine, they take place in well-separated steps in pyridoxamine (PM), pyridoxamine phosphate (PMP), and pyridoxal phosphate. It has been established that the ionization with a pK_a value of 3.7 is predominantly phenolic in origin in PM and PMP. A zwitterionic structure consistent with the earlier spectroscopic investigations is proposed for the vitamin B₆ compounds in neutral aqueous solution.     

Membrane potentials of human fibroblast strains in culture

With a simple technique, the membrane electro-physiology of mammalian fibroblasts in tissue culture can be explored with micro-electrodes. Measured in complete, serum-containing medium, the mean membrane potential for human diploid cell strains in between 70 and 75 millivolts.