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Journal article

A robust normalized local filter to estimate compositional heterogeneity directly from cryo-EM maps

Abstract:
Sphingolipid levels are crucial determinants of neurodegenerative disorders and therefore require tight regulation. The Orm protein family and ceramides inhibit the rate-limiting step of sphingolipid biosynthesis—the condensation of L-serine and palmitoyl-coenzyme A (CoA). The yeast isoforms Orm1 and Orm2 form a complex with the serine palmitoyltransferase (SPT). While Orm1 and Orm2 have highly similar sequences, they are differentially regulated, though the mechanistic details remain elusive. Here, we determine the cryoelectron microscopy structure of the SPT complex containing Orm2. Complementary in vitro activity assays and genetic experiments with targeted lipidomics demonstrate a lower activity of the SPT-Orm2 complex than the SPT-Orm1 complex. Our results suggest a higher inhibitory potential of Orm2, despite the similar structures of the Orm1- and Orm2-containing complexes. The high conservation of SPT from yeast to man implies different regulatory capacities for the three human ORMDL isoforms, which might be key for understanding their role in sphingolipid-mediated neurodegenerative disorders
Publication status:
Published
Peer review status:
Peer reviewed

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Institution:
University of Oxford
Role:
Author
ORCID:
0000-0002-6247-4063
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Institution:
University of Oxford
Role:
Author
ORCID:
0000-0003-1212-904X
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Role:
Author
ORCID:
0000-0002-9341-2295


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Funder identifier:
10.13039/100004440
Grant:
203141/Z/16/Z
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Funder identifier:
10.13039/501100000289
Grant:
C20724/A26752
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Funder identifier:
10.13039/501100004359
Grant:
2020-06413


Publisher:
Nature Research
Journal:
Nature Communications More from this journal
Volume:
14
Issue:
1
Pages:
5802-5802
Article number:
5802
Publication date:
2023-09-19
DOI:
EISSN:
2041-1723
ISSN:
2041-1723


Language:
English
Keywords:
Pubs id:
1536750
Local pid:
pubs:1536750
Source identifiers:
W4386847736
Deposit date:
2026-05-17
ARK identifier:
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