Optimal discrimination and classification of neuronal actionpotential waveforms from multiunit, multichannel recordings usingsoftware-based linear filters

Describes advanced protocols for the discrimination and classification of neuronal spike waveforms within multichannel electrophysiological recordings. The programs are capable of detecting and classifying the spikes from multiple, simultaneously active neurons, even in situations where there is a high degree of spike waveform superposition on the recording channels. The protocols are based on the derivation of an optimal linear filter for each individual neuron. Each filter is tuned to selectively respond to the spike waveform generated by the corresponding neuron, and to attenuate noise and the spike waveforms from all other neurons. The protocol is essentially an extension of earlier work (S. Andreassen et al., 1979; W.M. Roberts and D.K. Hartline, 1975; R.B. Stein et al., 1979). However, the protocols extend the power and utility of the original implementations in two significant respects. First, a general single-pass automatic template estimation algorithm was derived and implemented. Second, the filters were implemented within a software environment providing a greatly enhanced functional organization and user interface. The utility of the analysis approach was demonstrated on samples of multiunit electrophysiological recordings from the cricket abdominal nerve cord     

Quasi-isoplanatic radiation transfer through randomly movingparticles

An iterative solution of an improved forward-scattering approximation for the radiative-transfer equation is derived. The narrow-angle approximation is useful for optical and acoustic beam propagation in the ocean and the atmosphere, where particle sizes are much larger than the wavelength. The improved narrow-angle approximation is useful for a cluster of anisotropic scatterers, and when the cluster is subjected to winds or currents. The solution of the derived equation is sought in terms of uniformly convergent iteration series via the two-scale embedding technique. The lowest iterative of the technique provides an approximate solution that differs from the commonly used successive substitution technique because it takes into account some of the multiple scattering terms. An example of wave propagation through randomly moving particles, useful for remote sensing, is considered     

A method to improve the estimation of conduction velocitydistributions over a short segment of nerve

Accurate, noninvasive determination of the distribution of conduction velocities (DCV) among fibers of a peripheral nerve has the potential to improve both clinical diagnoses of pathology and longitudinal studies of the progress of disease or the efficacy of treatments. Current techniques rely on long distances of propagation to increase the amount of temporal dispersion in the compound signals and reduce the relative effect of errors in the forward model. The method described in this paper attempts to reduce errors in DCV estimation through transfer function normalization and, thereby, eliminate the need for long segments of nerve. Compound action potential (CAP) signals are recorded from several, equally spaced electrodes in an array spanning only a 10-cm length of nerve. Relative nerve-to-electrode transfer functions (NETF's) between the nerve and each of the array electrodes are estimated by comparing discrete Fourier transforms of the array signals. NETF's are normalized along the array so that waveform differences can be attributed to the effects of temporal dispersion between recordings, and more accurate DCV estimates can be calculated from the short nerve segment. The method is tested using simulated and real CAP data. DCV estimates are improved for simulated signals. The normalization procedure results in DCV's that qualitatively match those from the literature when used on actual CAP recordings.     

关于Hirota-Satsuma系统初值问题的局部和整体适定性

本文利用ＫＤＶ方程所对应的线性方程解所具有的光滑效应及压缩映像原理,得到了Ｈｉｒｏｔａ－Ｓａｔｓｕｍａ系统初值问题的局部和整体适定性结果．     

Overlapping B3Π0u ← X1Σ g/+ and 1Π1u ← X1Σ g/+ non-radiative characteristic of Br2 vapour in the wavelength region 505–541 nm

The vibronic vapour phase photoacoustic spectrum of Br₂ in the wavelength region 505–541 nm (19796–18480 cm⁻¹) has been recorded using microphone as well as pump-probe method. Discrete vibronic bands superimposed on a monotonically increasing continuum background towards the dissociation limit results from the overlapping B ³Π _0u ^/+ ← X ¹Σ _g ^/+ and ¹Π_1u ← X ¹Σ _g ^/+ electronic transitions. Vibronic bands originating from υ″=0 have been used to estimate the relative rate of non-radiative relaxation as a function of the excited state B ³Π_0u vibrational quantum number υ′. A comparison with the optical absorption spectroscopy of Br₂ leads to the identification of three broad spectral regions between 505 and 541 nm (19796 and 18480 cm⁻¹) on the basis of different non-radiative relaxation processes.     

Effect of the intermittent atmosphere on laser scintillations

The evolution of the scintillation index of a spherical wave propagating through randomly varying profiles of the strength and the smallest scale of turbulence is calculated. These parameters were taken to be jointly log normal along the range. The specific parameters of the probability-density function that were used were taken from stratospheric experiments conducted by the U.S. Air Force.     

NMR assignments and histone specificity of the ING2 PHD finger

The ING2 plant homeodomain (PHD) finger is recruited to the nucleosome through specific binding to histone H3 trimethylated at lysine 4 (H3K4me3). Here, we describe backbone and side chain assignments of the ING2 PHD finger, analyze its binding to the unmodified and modified histone and p53 peptides, and map the histone H3 and H3K4me3 binding sites based on chemical shift perturbation analysis. Copyright © 2009 John Wiley & Sons, Ltd.     

Stabilized phosphatidylinositol-5-phosphate analogues as ligands for the nuclear protein ING2: chemistry, biology, and molecular modeling

The interaction of PtdIns(5)P with the tumor suppressor protein ING2 has been implicated in the regulation of chromatin modification. To enhance the stability of PtdIns(5)P for studies of the biological role in vivo, two phosphatase-resistant moieties were used to replace the labile 5-phosphate. The total asymmetric synthesis of the 5-methylenephosphonate (MP) and 5-phosphothionate (PT) analogues of PtdIns(5)P is described herein, and the resulting metabolically stabilized lipid analogues were evaluated in three ways. First, liposomes containing either the dioleoyl MP or PT analogues bound to recombinant ING2 similar to liposomes containing dipalmitoyl PtdIns(5)P, indicating that the replacement of the hydrolyzable 5-phosphate group does not compromise the binding. Second, the dioleoyl MP and PT PtdIns(5)P analogues were equivalent to dipalmitoyl PtdIns(5)P in augmenting cell death induced by a DNA double-strand break in HT1080 cells. Finally, molecular modeling and docking of the MP or PT analogues to the C-terminus PtdInsP-binding region of ING2 (consisting of a PHD finger and a polybasic region) revealed a number of complementary surface and electrostatic contacts between the lipids and ING2.     

On the two-scale expansion of the fourth moment of a wave propagating in a random medium

A comprehensive and rigorous analysis of the prevalent version of the two-scale expansion used to solve the fourth-moment equation shows that it is not an asymptotic technique. The correct asymptotic version is derived and found to be analytically non-tractable. An elaborated interpretation to the correction terms used before is established and shows that an additional term of the same order was overlooked. The new expression which will improve the result in the scintillation peak is offered. The role of the small parameter of the problem is discussed.     

A new salicin derivative from the stem bark of Populus davidiana

Phytochemical study on the BuOH-soluble fraction of the stem bark of Populus davidiana resulted in the isolation of a new salicin derivative(1),named davidianoside.The structure was elucidated on the basis of extensive physicochemical and spectroscopic analyses.