Homology modeling and in vivo functional characterization of the zinc permeation pathway in a heavy metal P-type ATPase. (10th November 2018)
- Record Type:
- Journal Article
- Title:
- Homology modeling and in vivo functional characterization of the zinc permeation pathway in a heavy metal P-type ATPase. (10th November 2018)
- Main Title:
- Homology modeling and in vivo functional characterization of the zinc permeation pathway in a heavy metal P-type ATPase
- Authors:
- Lekeux, Gilles
Crowet, Jean-Marc
Nouet, Cécile
Joris, Marine
Jadoul, Alice
Bosman, Bernard
Carnol, Monique
Motte, Patrick
Lins, Laurence
Galleni, Moreno
Hanikenne, Marc - Abstract:
- Abstract : Three-dimensional modeling of the HMA4 protein in Arabidopsis reveals the zinc permeation pathway across the plasma membrane, and mutations in the pathway alter zinc and cadmium transport differently in plants. Abstract: The P1B ATPase heavy metal ATPase 4 (HMA4) is responsible for zinc and cadmium translocation from roots to shoots in Arabidopsis thaliana . It couples ATP hydrolysis to cytosolic domain movements, enabling metal transport across the membrane. The detailed mechanism of metal permeation by HMA4 through the membrane remains elusive. Here, homology modeling of the HMA4 transmembrane region was conducted based on the crystal structure of a ZntA bacterial homolog. The analysis highlighted amino acids forming a metal permeation pathway, whose importance was subsequently investigated functionally through mutagenesis and complementation experiments in plants. Although the zinc pathway displayed overall conservation among the two proteins, significant differences were observed, especially in the entrance area with altered electronegativity and the presence of a ionic interaction/hydrogen bond network. The analysis also newly identified amino acids whose mutation results in total or partial loss of the protein function. In addition, comparison of zinc and cadmium accumulation in shoots of A. thaliana complemented lines revealed a number of HMA4 mutants exhibiting different abilities in zinc and cadmium translocation. These observations could be instrumentalAbstract : Three-dimensional modeling of the HMA4 protein in Arabidopsis reveals the zinc permeation pathway across the plasma membrane, and mutations in the pathway alter zinc and cadmium transport differently in plants. Abstract: The P1B ATPase heavy metal ATPase 4 (HMA4) is responsible for zinc and cadmium translocation from roots to shoots in Arabidopsis thaliana . It couples ATP hydrolysis to cytosolic domain movements, enabling metal transport across the membrane. The detailed mechanism of metal permeation by HMA4 through the membrane remains elusive. Here, homology modeling of the HMA4 transmembrane region was conducted based on the crystal structure of a ZntA bacterial homolog. The analysis highlighted amino acids forming a metal permeation pathway, whose importance was subsequently investigated functionally through mutagenesis and complementation experiments in plants. Although the zinc pathway displayed overall conservation among the two proteins, significant differences were observed, especially in the entrance area with altered electronegativity and the presence of a ionic interaction/hydrogen bond network. The analysis also newly identified amino acids whose mutation results in total or partial loss of the protein function. In addition, comparison of zinc and cadmium accumulation in shoots of A. thaliana complemented lines revealed a number of HMA4 mutants exhibiting different abilities in zinc and cadmium translocation. These observations could be instrumental to design low cadmium-accumulating crops, hence decreasing human cadmium exposure. … (more)
- Is Part Of:
- Journal of experimental botany. Volume 70:Number 1(2019)
- Journal:
- Journal of experimental botany
- Issue:
- Volume 70:Number 1(2019)
- Issue Display:
- Volume 70, Issue 1 (2019)
- Year:
- 2019
- Volume:
- 70
- Issue:
- 1
- Issue Sort Value:
- 2019-0070-0001-0000
- Page Start:
- 329
- Page End:
- 341
- Publication Date:
- 2018-11-10
- Subjects:
- Arabidopsis -- HMA4 -- homology modeling -- in vivo imaging -- metal transport -- molecular dynamics -- P-type ATPase -- zinc
Botany -- Periodicals
Botany, Experimental -- Periodicals
Plant physiology -- Periodicals
580 - Journal URLs:
- http://ukcatalogue.oup.com/ ↗
http://jxb.oxfordjournals.org/ ↗ - DOI:
- 10.1093/jxb/ery353 ↗
- Languages:
- English
- ISSNs:
- 0022-0957
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4981.000000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 11874.xml