PubMed Health⌕ Search

PubMed · 1693092

Alternate methods of representing single-channel data.

Abstract

Clustering of dwell times in data from single-channel recordings, which is in excess of the value predicted from the probability density function (pdf) alone, provides restrictions on modeling schemes. Two methods, (a) the probability density function of the running median for groups of any size of sequential dwell times, and (b) the distribution of cumulative probabilities associated with dwell times separated by any lag, or the second cumulative probability distribution, are proposed as alternative representations of single-channel data; these methods are suitable for the detection of such clusters or modes. Simulation of three models with and without modes is done to test the efficacy of these methods. It is found that they often yield a better estimate of moding parameters than the methods of running mean pdf and autocorrelation.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

S V Ramanan, P R Brink. 1990. Alternate methods of representing single-channel data.. https://doi.org/10.1016/s0006-3495(90)82609-6

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

KEEP EXPLORING

Related citations

Charge inversion at high ionic strength studied by streaming currents.

We report charge inversion, the sign reversal of the effective surface charge in the presence of multivalent counterions, for the biologically relevant regimes of divalent ions and mixtures of monovalent and multivalent ions. Using streaming currents, the pressure-driven transport of countercharges in the diffuse layer, we find that charge inversion occurs in rectangular silica nanochannels at high concentrations of divalent ions. Strong monovalent screening is found to cancel charge inversion, restoring the original surface charge polarity. An analytical model based on ion correlations successfully describes our observations.

Ion Channels↗

Synthetic ion channels and pores (2004-2005).

This critical review covers synthetic ion channels and pores created between January 2004 and December 2005 comprehensively. The discussion of a rich collection of structural motifs may particularly appeal to organic, biological, supramolecular and polymer chemists. Functions addressed include ion selectivity and molecular recognition, as well as responsiveness to light, heat, voltage and membrane composition. The practical applications involved concern certain topics in medicinal chemistry (antibiotics, drug delivery), catalysis and sensing. An introduction to principles and methods is provided for the non-specialist; some new sources of inspiration from fields beyond chemistry are highlighted.

Ion Channels↗

Affinity of 1-aryl-1,2,3,4-tetrahydroisoquinoline derivatives to the ion channel binding site of the NMDA receptor complex.

A series of 1-aryl-1,2,3,4-tetrahydroisoquinoline and 8-methyl-1-aryl-1,2,3,4-tetrahydroisoquinoline derivatives was evaluated for affinity to the PCP binding site of the NMDA receptor complex. The (S)-configured tetrahydroisoquinoline derivative (S)-4 e x HCl bearing a 2-methylphenyl substituent in position 1 of the heterocyclic ring system and a methyl group in position 8 was found to exhibit the highest affinity among the derivatives with a K(i)-value of 0.0374 microM. In addition, this compound shows a remarkable enantioselectivity of binding by being almost 90 times more potent than the corresponding (R)-enantiomer (R)-4 e x HCl. Additionally, a convenient and efficient synthetic approach to racemic 1-aryl-1,2,3,4-tetrahydroisoquinoline derivatives is described.

Ion Channels↗