PubMed Health⌕ Search

PubMed · 14796655

MEMBRANE permeability.

Abstract

The source did not provide an abstract. Follow the original record for more information.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

1950-12-09. MEMBRANE permeability.. https://doi.org/10.1038/166987a0

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related citations

6-methylpyridyl for pyridyl substitution tunes the properties of fluorescent zinc sensors of the Zinpyr family.

To prepare fluorescent zinc sensors with binding affinities lower than that of the parent 9-(o-carboxyphenyl)-2,7-dichloro-4,5-bis(bis(2-pyridylmethyl)methylaminomethyl)-6-hydroxy-3-xanthenone (ZP1), dimethylated and tetramethylated derivatives were synthesized having either two or four of the pyridyl subunits methylated at the 6-position. Like the parent ZP1, both Me(2)ZP1 and Me(4)ZP1 exhibit increased fluorescence in the presence of Zn(2+). The integrated emission of Me(2)ZP1 increases 4-fold in the presence of excess zinc, whereas Me(4)ZP1 displays 2.5-fold enhanced fluorescence for Zn(2+). Methylating the 6-positions of the pyridyl rings raises the dissociation constant of the sensors and lowers the pK(a) values associated with the tertiary amine ligands in a systematic manner. The properties of the dimethylated Me(2)ZP1 dye resemble those of ZP1, but the tetramethylated Me(4)ZP1 differs greatly from ZP1 in terms of its brightness, affinity toward Zn(2+), exchange kinetics, and metal sensitivity. Both Me(2)ZP1 and Me(4)ZP1 can enter HeLa cells and signal the presence of Zn(2+). Staining caused by both dyes is punctate, with localization patterns resembling that observed for ZP1.

Cell Membrane Permeability↗

The amplitude distribution of release events through a fusion pore.

Neurotransmitters, hormones, or dyes may be released from vesicles via a fusion pore, rather than by full fusion of the vesicle with the plasma membrane. If the lifetime of the fusion pore is comparable to the time required for the substance to exit the vesicle, only a fraction of the total vesicle content may be released during a single pore opening. Assuming 1), fusion pore lifetimes are exponentially distributed (tauP), as expected for simple single channel openings, and 2), vesicle contents are lost through the fusion pore with an exponential time course (tauD), we derive an analytical expression for the probability density function of the fraction of vesicle content released (F): dP/dF=A (1-F)(A-1), where A=tauD/tauP. If A>1, the maximum of the distribution is at F=0; if A<1, the maximum is at F=1; if A=1, the distribution is perfectly flat. Thus, the distribution never has a peak in the middle (0<F<1). This should be considered when interpreting the distribution of miniature synaptic currents, or the fraction of FM dye molecules lost during a single fusion pore opening event.

Cell Membrane Permeability↗

Phytotoxicity of lanthanum in rice in haplic acrisols and cambisols.

Growth and physiological responses of rice to lanthanum were studied to elucidate the function of lanthanum in plants and its critical concentration relative to environmental safety. Shoot La content increased with the increasing added La concentrations. When shoot La content exceeded a toxic value, plant growth and chlorophyll a/b decreased and peroxidase (POD) activity, cell membrane permeability, and content of proline in the leaf increased. Leaf chlorophyll a/b and POD activity might provide useful criteria for early diagnoses of phytotoxicity of soil contaminated by La. In the present study, the critical concentration of La for rice relative to environmental safety was suggested to be 42.03 mg kg(-1) in red soil and 83.33 mg kg(-1) in paddy soil.

Cell Membrane Permeability↗