Evidence map›Paper›PMID 30694671›Full record

ArticleThe journal of physical chemistry. B2019

Exposing the Nucleation Site in α-Helix Folding: A Joint Experimental and Simulation Study.

Arusha Acharyya, Yunhui Ge, Haifan Wu, William F DeGrado, Vincent A Voelz, Feng Gai

Abstract read
In one paragraph

Article in The journal of physical chemistry. B, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

13 citing papers in PubMed.

  1. Forces behind N- and C-capping of peptidic helices.Chemical communications (Cambridge, England) · 2026
    Article
  2. Article
  3. Article
  4. Dual-Capped Helical Interface Mimics.Journal of the American Chemical Society · 2024
    Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Markov State Models to Elucidate Ligand Binding Mechanism.Methods in molecular biology (Clifton, N.J.) · 2021
    Review
  12. Article
  13. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Arusha AcharyyaDepartment of Chemistry , University of Pennsylvania , Philadelphia , Pennsylvania 19104 , United States.
Yunhui GeDepartment of Chemistry , Temple University , Philadelphia , Pennsylvania 19122 , United States.
Haifan WuDepartment of Pharmaceutical Chemistry , University of California , San Francisco , California 94158 , United States.ORCID 0000-0002-2050-9950
William F DeGradoDepartment of Pharmaceutical Chemistry , University of California , San Francisco , California 94158 , United States.ORCID 0000-0003-4745-263X
Vincent A VoelzDepartment of Chemistry , Temple University , Philadelphia , Pennsylvania 19122 , United States.ORCID 0000-0002-1054-2124
Feng GaiDepartment of Chemistry , University of Pennsylvania , Philadelphia , Pennsylvania 19104 , United States.ORCID 0000-0003-1621-7119

Funding

NRSA Training CoreTL1TR001871 · NCATS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI KANAYA, ALKA M., SOMSOUK, MA · 2016 to 2025
$10.1M
Deciphering the relationship between structure, dynamics and function in helical bundle proteinsR35GM122603 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI WILLIAM DEGRADO · 2017 to 2026
$7.1M
ULTRAFAST OPTICAL PROCESSES LABORATORYP41GM104605 · NIGMS · UNIVERSITY OF PENNSYLVANIA · PI GAI, FENG · 2012 to 2017
$5.6M
Markov State Model approaches for folding, binding and designR01GM123296 · NIGMS · TEMPLE UNIV OF THE COMMONWEALTH · PI VOELZ, VINCENT · 2017 to 2025
$3.1M
Computer Cluster for Computational Biology and BiophysicsS10OD020095 · OD · TEMPLE UNIV OF THE COMMONWEALTH · PI LEVY, RONALD · 2015 to 2015
$442k
NCATS NIH HHS TL1 TR001871NIGMS NIH HHS P41 GM104605NIGMS NIH HHS R01 GM123296NIGMS NIH HHS R35 GM122603NIH HHS S10 OD020095
6 · The paper itself

Abstract

One of the fundamental events in protein folding is α-helix formation, which involves sequential development of a series of helical hydrogen bonds between the backbone C═O group of residues i and the -NH group of residues i + 4. While we now know a great deal about α-helix folding dynamics, a key question that remains to be answered is where the productive helical nucleation event occurs. Statistically, a helical nucleus (or the first helical hydrogen-bond) can form anywhere within the peptide sequence in question; however, the one that leads to productive folding may only form at a preferred location. This consideration is based on the fact that the α-helical structure is inherently asymmetric, due to the specific alignment of the helical hydrogen bonds. While this hypothesis is plausible, validating it is challenging because there is not an experimental observable that can be used to directly pinpoint the location of the productive nucleation process. Therefore, in this study we combine several techniques, including peptide cross-linking, laser-induced temperature-jump infrared spectroscopy, and molecular dynamics simulations, to tackle this challenge. Taken together, our experimental and simulation results support an α-helix folding mechanism wherein the productive nucleus is formed at the N-terminus, which propagates toward the C-terminal end of the peptide to yield the folded structure. In addition, our results show that incorporation of a cross-linker can lead to formation of differently folded conformations, underscoring the need for all-atom simulations to quantitatively assess the proposed cross-linking design.

Indexed as

Molecular Dynamics SimulationProtein FoldingKineticsPeptidesProtein Conformation, alpha-HelicalTemperaturePeptides

Identifiers

PMID30694671
PMCPMC6497059

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Registered trials

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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.