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2 produkter
2 produkter
1 091 kr
Skickas inom 10-15 vardagar
The most critical event in chemical cell to cell communications is the conversion of the chemical signal into the primary response of the receiving cell. In the case of cholinergic cell to cell communication, i. e. in cholinergic nerve-nerve and nerve- muscle systems, a single molecule, namely the nicotinic acetyl- choline receptor is responsible for both signal reception and primary response: Through binding of the neurotransmitter acetyl- choline released from the associated nerve ending, the receptor receives the chemical message. Short-lived openings of the recep- tor-integral ion channel constitute the initial reaction to this stimulation, i. e. the primary response. This integration of the receiving and the responsive unit into a single protein structure seems to be typical for transmi tter-acti vated ion channel pro- teins of many excitable cells including those of the central ner- vous system. Elucidation of the mechansim of action of the acetylcholine receptor is of interest, therefore, not only for cholinergic cell to cell communications but, even more impor- tantly, as a general model for the less accessible neurotransmit- ter receptors of the central nervous system.While the basic reactions in the, course of cholinergic cell to cell communication and the molecular components involved are rather well understood, a molecular mechanism for cholinergic ex- ci tation has not yet been established.
1 585 kr
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This workshop was the second of this series held on the island of santorini in the Cycladic Sea. The first one ("Mechanism of Action of the Nicotinic Acetylcholine Receptor", NATO ASI Se ries H, vol. 10) took place in May 1986 and focused on what was at the time the best studied of all neuroreceptors. This second one, held only two years later, demonstrates the im mense progress achieved since then in the field of neurorecep tors and ion channels. Molecular cloning techniques have now made available the primary structures of a whole array of ion channel proteins, and this in turn has shed light on some gen eral principles of the structure-function relationships of these central elements of intercellular communication. The purpose of this workshop was to explore the common ele ments in gene and protein structure of already cloned ion channel proteins, and to assess the status of other cloning projects in progress. It explicitly focused on very recently published and unpublished results. All participants kept to these goals thereby demonstrating the very value of such work shops for the progress of science.