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W K Wang

Publications and source records attributed to W K Wang.

61 records · Page 4Linked to original sources

The relaxation of ions can contribute additional "state" during gating current measurement.

A transient time is needed for a potential step to travel through the solution between the metal electrode and the membrane. The effects of the double layer that exists at the electrode-solution interface may cause a delay for the signal reaching the surface of the membrane to initiate any voltage dependent reaction. The process by which the ions of the solution redistribute themselves is described by a relaxation model. The relaxation time is related to the resistance of the solution and the equivalent capacitance of the diffuse double layer. The theory is then applied to the experiments that measured the gating process of nerve membrane. The delay time of the rise in the sodium conductance on polarization is calculated for various polarized potentials and holding potentials and the numerical results can explain the experimental data without using the multi-state kinetic models. It indicates that the relaxation time of the solution should be taken into consideration for any membrane experiment with time courses of similar order.

Animals↗

Membrane potential and active transport--an information theory approach.

A membrane potential stabilizing mechanism is proposed. Permeability is portrayed as controlled by a potential sensor. The active transport system is suggested to be a Maxwell demon able to recognize different ions, and modulate their passage into and out of the cell, without apparent reliance on energy. The idea that information is equivalent to entropy is used to resolve that paradox and construct a model of the active transport system. The non-steady ionic state of muscle cell is deduced; that ionic concentration may determine the condition of muscle is also suggested.

Animals↗

Role of the CCR5 delta 32 allele in resistance to HIV-1 infection in west Africa.

OBJECTIVE: To determine the frequency of the mutant CCR5 delta 32 allele in high-risk HIV-seronegative Africans as compared with the general African population, and to assess its in vitro protective efficacy against HIV-1 infection. STUDY DESIGN: In the homozygous form, the CCR5 delta 32 allele confers resistance to macrophage-tropic (M-tropic) strains of HIV-1. Assuming that genetic characteristics favoring HIV resistance would prevail in a high-risk HIV-seronegative population, we examined the CCR5 genotypes of female commercial sex workers (CSWs) from Dakar, Senegal, who have remained uninfected for an elongated period. METHODS: The CCR5 genetic profile of study participants was determined by polymerase chain reaction (PCR) amplification of genomic DNA followed by sequencing. Peripheral blood mononuclear cells (PBMCs) were infected with different strains of HIV-1 and monitored by p24 enzyme-linked immunosorbent assay (ELISA). RESULTS: We confirmed the presence of two CCR5wt/delta 32 genotypes among 139 individuals (1.44%). PBMCs from these 2 heterozygous individuals were also found to be less susceptible to in vitro infection by an M-tropic HIV-1 primary isolate. CONCLUSIONS: Evidence was found of an increased prevalence of the CCR5wt/delta 32 genotype in a high-risk HIV-seronegative cohort in West Africa. Furthermore, reduced susceptibility to HIV-1 infection among heterozygous individuals supports a role for 32-bp CCR5 deletion in HIV-1 resistance.

Acquired Immunodeficiency Syndrome↗