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Chasing acyl carrier protein through a catalytic cycle of lipid A production.

Publication ,  Journal Article
Masoudi, A; Raetz, CRH; Zhou, P; Pemble, CW
Published in: Nature
January 16, 2014

Acyl carrier protein represents one of the most highly conserved proteins across all domains of life and is nature's way of transporting hydrocarbon chains in vivo. Notably, type II acyl carrier proteins serve as a crucial interaction hub in primary cellular metabolism by communicating transiently between partner enzymes of the numerous biosynthetic pathways. However, the highly transient nature of such interactions and the inherent conformational mobility of acyl carrier protein have stymied previous attempts to visualize structurally acyl carrier protein tied to an overall catalytic cycle. This is essential to understanding a fundamental aspect of cellular metabolism leading to compounds that are not only useful to the cell, but also of therapeutic value. For example, acyl carrier protein is central to the biosynthesis of the lipid A (endotoxin) component of lipopolysaccharides in Gram-negative microorganisms, which is required for their growth and survival, and is an activator of the mammalian host's immune system, thus emerging as an important therapeutic target. During lipid A synthesis (Raetz pathway), acyl carrier protein shuttles acyl intermediates linked to its prosthetic 4'-phosphopantetheine group among four acyltransferases, including LpxD. Here we report the crystal structures of three forms of Escherichia coli acyl carrier protein engaging LpxD, which represent stalled substrate and liberated products along the reaction coordinate. The structures show the intricate interactions at the interface that optimally position acyl carrier protein for acyl delivery and that directly involve the pantetheinyl group. Conformational differences among the stalled acyl carrier proteins provide the molecular basis for the association-dissociation process. An unanticipated conformational shift of 4'-phosphopantetheine groups within the LpxD catalytic chamber shows an unprecedented role of acyl carrier protein in product release.

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Published In

Nature

DOI

EISSN

1476-4687

Publication Date

January 16, 2014

Volume

505

Issue

7483

Start / End Page

422 / 426

Location

England

Related Subject Headings

  • Protein Conformation
  • Protein Binding
  • Models, Molecular
  • Lipid A
  • Hydrolysis
  • General Science & Technology
  • Escherichia coli
  • Crystallography, X-Ray
  • Biocatalysis
  • Acyltransferases
 

Citation

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Masoudi, A., Raetz, C. R. H., Zhou, P., & Pemble, C. W. (2014). Chasing acyl carrier protein through a catalytic cycle of lipid A production. Nature, 505(7483), 422–426. https://doi.org/10.1038/nature12679
Masoudi, Ali, Christian R. H. Raetz, Pei Zhou, and Charles W. Pemble. “Chasing acyl carrier protein through a catalytic cycle of lipid A production.Nature 505, no. 7483 (January 16, 2014): 422–26. https://doi.org/10.1038/nature12679.
Masoudi A, Raetz CRH, Zhou P, Pemble CW. Chasing acyl carrier protein through a catalytic cycle of lipid A production. Nature. 2014 Jan 16;505(7483):422–6.
Masoudi, Ali, et al. “Chasing acyl carrier protein through a catalytic cycle of lipid A production.Nature, vol. 505, no. 7483, Jan. 2014, pp. 422–26. Pubmed, doi:10.1038/nature12679.
Masoudi A, Raetz CRH, Zhou P, Pemble CW. Chasing acyl carrier protein through a catalytic cycle of lipid A production. Nature. 2014 Jan 16;505(7483):422–426.
Journal cover image

Published In

Nature

DOI

EISSN

1476-4687

Publication Date

January 16, 2014

Volume

505

Issue

7483

Start / End Page

422 / 426

Location

England

Related Subject Headings

  • Protein Conformation
  • Protein Binding
  • Models, Molecular
  • Lipid A
  • Hydrolysis
  • General Science & Technology
  • Escherichia coli
  • Crystallography, X-Ray
  • Biocatalysis
  • Acyltransferases