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Journal article : Review

Novel structural insights at the extracellular plant-pathogen interface

Abstract:
Plant pathogens represent a critical threat to global agriculture and food security, particularly under the pressures of climate change and reduced agrochemical use. Most plant pathogens initially colonize the extracellular space or apoplast and understanding the host-pathogen interactions that occur here is vital for engineering sustainable disease resistance in crops. Structural biology has played important roles in elucidating molecular mechanisms underpinning plant-pathogen interactions but only few studies have reported structures of extracellular complexes. This article highlights these resolved extracellular complexes by describing the insights gained from the solved structures of complexes consisting of CERK1-chitin, FLS2-flg22-BAK1, RXEG1-XEG1-BAK1 and PGIP2-FpPG. Finally, we discuss the potential of AI-based structure prediction platforms like AlphaFold as an alternative hypothesis generator to rapidly advance our molecular understanding of plant pathology and develop novel strategies to increase crop resilience against disease.
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1016/j.pbi.2024.102629

Authors

More by this author
Institution:
University of Oxford
Division:
MPLS
Department:
Biology
Role:
Author
More by this author
Institution:
University of Oxford
Division:
MPLS
Department:
Biology
Sub department:
Plant Sciences
Oxford college:
Somerville College
Role:
Author
ORCID:
0000-0002-3692-7487


More from this funder
Funder identifier:
https://ror.org/0472cxd90
Grant:
101019324


Publisher:
Elsevier
Journal:
Current Opinion in Plant Biology More from this journal
Volume:
82
Article number:
102629
Place of publication:
England
Publication date:
2024-09-18
Acceptance date:
2024-08-29
DOI:
EISSN:
1879-0356
ISSN:
1369-5266
Pmid:
39299144


Language:
English
Keywords:
Subtype:
Review
Pubs id:
2032280
Local pid:
pubs:2032280
Deposit date:
2025-04-29
ARK identifier:

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