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Copper chaperones. The concept of conformational control in the metabolism of copper

FEBS letters, 2013-06, Vol.587 (13), p.1902-1910

Palumaa, Peep

2013

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Copper(II)-binding equilibria in human blood

Scientific reports, 2020-03, Vol.10 (1), p.5686-5686, Article 5686

2020

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Metabolism of copper and possibilities for its regulation

Proceedings of the Estonian Academy of Sciences, 2023-01, Vol.72 (4), p.382-392

Palumaa, P

2023

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In situ fibrillizing amyloid-beta 1-42 induces neurite degeneration and apoptosis of differentiated SH-SY5Y cells

PloS one, 2017-10, Vol.12 (10), p.e0186636

2017

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Formation of [4Fe-4S] Clusters in the Mitochondrial Iron–Sulfur Cluster Assembly Machinery

Journal of the American Chemical Society, 2014-11, Vol.136 (46), p.16240-16250

2014

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Copper(I)-binding properties of de-coppering drugs for the treatment of Wilson disease. α-Lipoic acid as a potential anti-copper agent

Scientific reports, 2018-01, Vol.8 (1), p.1463-9, Article 1463

2018

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Human superoxide dismutase 1 (hSOD1) maturation through interaction with human copper chaperone for SOD1 (hCCS)

Proceedings of the National Academy of Sciences - PNAS, 2012-08, Vol.109 (34), p.13555-13560

2012

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Mitochondrial Copper(I) Transfer from Cox17 to Sco1 Is Coupled to Electron Transfer

Proceedings of the National Academy of Sciences - PNAS, 2008-05, Vol.105 (19), p.6803-6808

2008

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Evaluation of Zn2+- and Cu2+-Binding Affinities of Native Cu,Zn-SOD1 and Its G93A Mutant by LC-ICP MS

Molecules (Basel, Switzerland), 2022-05, Vol.27 (10), p.3160

2022

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In vitro fibrillization of Alzheimer’s amyloid-β peptide (1-42)

AIP advances, 2015-09, Vol.5 (9), p.092401-092401-12

2015

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α-Lipoic acid: a potential regulator of copper metabolism in Alzheimer's disease

Frontiers in molecular biosciences, 2024-09, Vol.11, p.1451536

2024

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Copper(II) partially protects three histidine residues and the N‐terminus of amyloid‐β peptide from diethyl pyrocarbonate (DEPC) modification

FEBS open bio, 2020-06, Vol.10 (6), p.1072-1081

2020

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Metabolism of copper and possibilities for its regulation/Vase metabolism ja selle reguleerimise voimalused

Proceedings of the Estonian Academy of Sciences, 2023-12, Vol.72 (4), p.382

Palumaa, Peep

2023

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Insulin Fibrillization at Acidic and Physiological pH Values is Controlled by Different Molecular Mechanisms

The Protein Journal, 2015-12, Vol.34 (6), p.398-403

2015

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A Structural-Dynamical Characterization of Human Cox17

The Journal of biological chemistry, 2008-03, Vol.283 (12), p.7912-7920

2008

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Mercury and Alzheimer's Disease: Hg(II) Ions Display Specific Binding to the Amyloid-β Peptide and Hinder Its Fibrillization

Biomolecules (Basel, Switzerland), 2020-01, Vol.10 (1), p.44

2020

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Direct Competition of ATCUN Peptides with Human Serum Albumin for Copper(II) Ions Determined by LC-ICP MS

ACS omega, 2023-09, Vol.8 (37), p.33912-33919

2023

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A Hint for the Function of Human Sco1 from Different Structures

Proceedings of the National Academy of Sciences - PNAS, 2006-06, Vol.103 (23), p.8595-8600

2006

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Metal-binding mechanism of Cox17, a copper chaperone for cytochrome c oxidase

Biochemical journal, 2004-08, Vol.382 (Pt 1), p.307-314

2004

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Human Sco1 functional studies and pathological implications of the P174L mutant

Proceedings of the National Academy of Sciences - PNAS, 2007-01, Vol.104 (1), p.15-20

2007

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Oxidative switches in functioning of mammalian copper chaperone Cox17

Biochemical journal, 2007-11, Vol.408 (1), p.139-148

2007

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Organization and Assembly of Metal-Thiolate Clusters in Epithelium-specific Metallothionein-4

The Journal of biological chemistry, 2006-05, Vol.281 (21), p.14588-14595

2006

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Affinity gradients drive copper to cellular destinations

Nature (London), 2010-06, Vol.465 (7298), p.645-648

2010

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Biological redox switches

Antioxidants & redox signaling, 2009-05, Vol.11 (5), p.981-983

Palumaa, Peep

2009

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α-Lipoic Acid Has the Potential to Normalize Copper Metabolism, Which Is Dysregulated in Alzheimer's Disease

Journal of Alzheimer's disease, 2022-01, Vol.85 (2), p.715-728

2022

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Copper chaperones. The concept of conformational control in the metabolism of copper

Copper(II)-binding equilibria in human blood

Metabolism of copper and possibilities for its regulation

In situ fibrillizing amyloid-beta 1-42 induces neurite degeneration and apoptosis of differentiated SH-SY5Y cells

Formation of [4Fe-4S] Clusters in the Mitochondrial Iron–Sulfur Cluster Assembly Machinery

Copper(I)-binding properties of de-coppering drugs for the treatment of Wilson disease. α-Lipoic acid as a potential anti-copper agent

Human superoxide dismutase 1 (hSOD1) maturation through interaction with human copper chaperone for SOD1 (hCCS)

Mitochondrial Copper(I) Transfer from Cox17 to Sco1 Is Coupled to Electron Transfer

Evaluation of Zn2+- and Cu2+-Binding Affinities of Native Cu,Zn-SOD1 and Its G93A Mutant by LC-ICP MS

In vitro fibrillization of Alzheimer’s amyloid-β peptide (1-42)

α-Lipoic acid: a potential regulator of copper metabolism in Alzheimer's disease

Copper(II) partially protects three histidine residues and the N‐terminus of amyloid‐β peptide from diethyl pyrocarbonate (DEPC) modification

Metabolism of copper and possibilities for its regulation/Vase metabolism ja selle reguleerimise voimalused

Insulin Fibrillization at Acidic and Physiological pH Values is Controlled by Different Molecular Mechanisms

A Structural-Dynamical Characterization of Human Cox17

Mercury and Alzheimer's Disease: Hg(II) Ions Display Specific Binding to the Amyloid-β Peptide and Hinder Its Fibrillization

Direct Competition of ATCUN Peptides with Human Serum Albumin for Copper(II) Ions Determined by LC-ICP MS

A Hint for the Function of Human Sco1 from Different Structures

Metal-binding mechanism of Cox17, a copper chaperone for cytochrome c oxidase

Human Sco1 functional studies and pathological implications of the P174L mutant

Oxidative switches in functioning of mammalian copper chaperone Cox17

Organization and Assembly of Metal-Thiolate Clusters in Epithelium-specific Metallothionein-4

Affinity gradients drive copper to cellular destinations

Biological redox switches

α-Lipoic Acid Has the Potential to Normalize Copper Metabolism, Which Is Dysregulated in Alzheimer's Disease

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