Evidence map›Paper›PMID 40737324›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2025

Identification of an on-pathway intermediate illuminates the kinetic competition between protein folding and misfolding.

Qing Luan, Patricia L Clark

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

2 authors.

Qing LuanDepartment of Chemistry and Biochemistry, University of Notre Dame, Notre Dame, IN 46556.ORCID 0009-0002-6286-291X
Patricia L ClarkDepartment of Chemistry and Biochemistry, University of Notre Dame, Notre Dame, IN 46556.ORCID 0000-0001-5462-8248

Funding

Decoding the regulation of protein folding by synonymous codon usageDP1GM146256 · NIGMS · UNIVERSITY OF NOTRE DAME · PI CLARK, PATRICIA LOUISE · 2021 to 2025
$5.5M
Integrative computational framework for pattern mining in big -omics data: linking synonymous codon usage to protein biogenesisR01GM120733 · NIGMS · UNIVERSITY OF NOTRE DAME · PI CLARK, PATRICIA LOUISE, EMRICH, SCOTT · 2016 to 2019
$1.1M
Upgraded circular dichroism spectropolarimeter for Notre Dame Biophysics Instrumentation Core FacilityS10OD036273 · OD · UNIVERSITY OF NOTRE DAME · PI CLARK, PATRICIA LOUISE · 2024 to 2024
$107k
NIGMS NIH HHS DP1 GM146256NIGMS NIH HHS R01 GM120733NIH HHS S10 OD036273ODCDC CDC HHS S10 OD036273
6 · The paper itself

Abstract

Our current understanding of protein folding is based predominantly on studies of small (<150 aa) proteins that refold reversibly from a chemically denatured state. However, as protein length increases so does the competition between off-pathway misfolding and on-pathway folding, creating a more complex energy landscape ("folding funnel"). Little is known about how intermediates populated during the folding of larger proteins affect navigation of this more complex landscape. Previously, we reported extremely slow folding rates for the 539 aa β-helical passenger domain of pertactin (P.69T), including conditions that favor the formation of a kinetically trapped, off-pathway partially folded state (PFS). Existence of an on-pathway intermediate for P.69T folding was speculated but its characterization remained elusive. In this work, we exploited the extremely slow kinetics of PFS unfolding to develop a double-jump "denaturant challenge" assay. With this assay, we identified a transient unfolding intermediate, PFS*, that adopts a similar structure to PFS, including C-terminal folded structure and a disordered N terminus, yet unfolds much more quickly than PFS. Additional experiments revealed that PFS* also functions as an on-pathway intermediate for P.69T folding. Collectively, these results support a C-to-N-terminal model for P.69T folding, with folding initiated in the C-terminus with the rate-limiting formation of the transient on-pathway PFS* intermediate, which sits at the junction of the kinetic competition between folding and misfolding. Notably, processive folding from C-to-N terminus also occurs during C-to-N-terminal translocation of P.69T across the bacterial outer membrane. These results illuminate the crucial role of kinetics when navigating a complex energy landscape for protein folding.

Indexed as

Bacterial Outer Membrane ProteinsProtein FoldingKineticsProtein ConformationBacterial Outer Membrane Proteinsautotransporterenergy landscapefolding funnelparallel β-helix

Identifiers

PMID40737324
PMCPMC12337298

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.