David J. Adams

Prof. David J. Adams

Faculty of Science, Medicine and Health, University of Wollongong, Wollongong, New South Wales, Australia
orcid
Distinguished Professor, University of Wollongong

Research Focus & Metrics

Academic Career Length

51Years (1976-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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3 February 2021 in Nature Reviews Drug Discovery
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MMMarkus Muttenthaler
Markus Muttenthaler
Glenn KingGlenn King
Glenn King
David J. AdamsDavid J. Adams
David J. Adams
PAPaul Alewood
Paul Alewood

1 October 1989 in The FASEB Journal
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David J. AdamsDavid J. Adams
David J. Adams
JBJoseph Barakeh
Joseph Barakeh
RLRachel Laskey
Rachel Laskey
CBCornelis Van Breemen
Cornelis Van Breemen

1 May 1980 in Journal of General Physiology
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TDT M Dwyer
T M Dwyer
David J. AdamsDavid J. Adams
David J. Adams
BHB Hille
B Hille
The relative permeability of endplate channels to many organic cations was determined by reversal-potential criteria. Endplate currents induced by iontophoretic "puffs" of acetylcholine were studied by a Vaseline gap, voltage clamp method in cut muscle fibers. Reversal potential changes were measured as the NaCl of the bathing medium was replaced by salts of organic cations, and permeability ratios relative to Na+ ions were calculated from the Goldman-Hodgkin-Katz equation. 40 small monovalent organic cations had permeability ratios larger than 0.1. The most permeant including NH4+, hydroxylamine, hydrazine, methylamine, guanidine, and several relatives of guanidine had permeability ratios in the range 1.3--2.0. However, even cations such as imidazole, choline, tris(hydroxymethyl)aminomethane, triethylamine, and glycine methylester were appreciably permeant with permeability ratios of 0.13--0.95. Four compounds with two charged nitrogen groups were also permeant. Molecular models of the permeant ions suggest that the smallest cross-section of the open pore must be at least as large as a square, 6.5 A x 6.5 A. Specific chemical factors seem to be less important than access or friction in determining the ionic selectivity of the endplate channel.

8 June 2010 in Angewandte Chemie International Edition
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RCRichard Clark
Richard Clark
JJJonas Jensen
Jonas Jensen
SNSimon T. Nevin
Simon T. Nevin
BCBrid P. Callaghan
Brid P. Callaghan
David J. AdamsDavid J. Adams
David J. Adams
DCDavid Craik
David Craik

1 May 1980 in Journal of General Physiology
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David J. AdamsDavid J. Adams
David J. Adams
TDT M Dwyer
T M Dwyer
BHB Hille
B Hille
The relative permeability of endplate channels to monovalent and divalent metal ions was determined from reversal potentials. Thallium is the most permeant ion with a permeability ratio relative to Na+ of 2.5. The selectivity among alkali metals is weak with a sequence, Cs+ greater than Rb+ greater than K+ greater than Na+ greater than Li+, and permeability ratios of 1.4, 1.3, 1.1, 1.0, and 0.9. The selectivity among divalent ions is also weak, with a sequence for alkaline earths of Mg++ greater than Ca++ greater than Ba++ greater than Sr++. The transition metal ions Mn++, Co++, Ni++, Zn++, and Cd++ are also permeant. Permeability ratios for divalent ions decreased as the concentration of divalent ion was increased in a manner consistent with the negative surface potential theory of Lewis (1979 J. Physiol. (Lond.). 286: 417--445). With 20 mM XCl2 and 85.5 mM glucosamine.HCl in the external solution, the apparent permeability ratios for the alkaline earth cations (X++) are in the range 0.18--0.25. Alkali metal ions see the endplate channel as a water-filled, neutral pore without high-field-strength sites inside. Their permeability sequence is the same as their aqueous mobility sequence. Divalent ions, however, have a permeability sequence almost opposite from their mobility sequence and must experience some interaction with groups in the channel. In addition, the concentrations of monovalent and divalent ions are increased near the channel mouth by a weak negative surface potential.

1 March 1980 in Annual Review of Neuroscience
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David J. AdamsDavid J. Adams
David J. Adams
SSS J Smith
S J Smith
STS H Thompson
S H Thompson