Evidence map›Paper›PMID 30133301›Full record

ArticleThe journal of physical chemistry. B2018

Complex Folding Landscape of Apomyoglobin at Acidic pH Revealed by Ultrafast Kinetic Analysis of Core Mutants.

Takuya Mizukami, Ming Xu, Ruzaliya Fazlieva, Valentina E Bychkova, Heinrich Roder

Abstract read
In one paragraph

Article in The journal of physical chemistry. B, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

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3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

  1. Influence of α-Helical Content on the Thermodiffusion of Apomyoglobin.Langmuir : the ACS journal of surfaces and colloids · 2025
    Article
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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

5 authors.

Takuya MizukamiMolecular Therapeutics Program , Fox Chase Cancer Center , Philadelphia , Pennsylvania 19111 , United States.
Ming XuMolecular Therapeutics Program , Fox Chase Cancer Center , Philadelphia , Pennsylvania 19111 , United States.
Ruzaliya FazlievaMolecular Therapeutics Program , Fox Chase Cancer Center , Philadelphia , Pennsylvania 19111 , United States.
Valentina E BychkovaLaboratory of Protein Physics , Institute of Protein Science, Russian Academy of Sciences , Pushchino , Moscow Region 142290 , Russia.
Heinrich RoderMolecular Therapeutics Program , Fox Chase Cancer Center , Philadelphia , Pennsylvania 19111 , United States.ORCID 0000-0003-1860-2491

Funding

WORD PROCESSING CENTER--COREP30CA006927 · NCI · RESEARCH INST OF FOX CHASE CAN CTR · PI Dietmar J Kappes · 1985 to 2026
$138.8M
Structural Plasticity and Functional Interactions of the Signaling Adapter NHERFR01GM116911 · NIGMS · RESEARCH INST OF FOX CHASE CAN CTR · PI RODER, HEINRICH · 2016 to 2019
$1.6M
NCI NIH HHS P30 CA006927NIGMS NIH HHS R01 GM116911
6 · The paper itself

Abstract

Under mildly acidic conditions (pH 4-4.5) apomyoglobin (apoMb) adopts a partially structured equilibrium state ( M-state) that structurally resembles a kinetic intermediate encountered at a late stage of folding to the native structure at neutral pH. We have previously reported that the M-state is formed rapidly (<1 ms) via a multistate process and thus offers a unique opportunity for exploring early stages of folding by both experimental and computational techniques. In order to gain structural insight into intermediates and barriers at the residue level, we studied the folding/unfolding kinetics of 12 apoMb mutants at pH 4.2 using fluorescence-detected ultrafast mixing techniques. Global analysis of the submillisecond folding/unfolding kinetics vs urea concentration for each variant, based on a sequential four-state mechanism ( U ⇔ I ⇔ L ⇔ M), allowed us to determine elementary rate constants and their dependence on urea concentration for most transitions. Comparison of the free energy diagrams constructed from the kinetic data of the mutants with that of wild-type apoMb yielded quantitative information on the effects of mutations on the free energy (ΔΔ G) of both intermediates and the first two kinetic barriers encountered during folding. Truncation of conserved aliphatic side chains on helices A, G, and H gives rise to a stepwise increase in ΔΔ G as the protein advances from U toward M, consistent with progressive stabilization of native-like contacts within the primary core of apoMb. Helix-helix contacts in the primary core contribute little to the first folding barrier ( U ⇔ I) and thus are not required for folding initiation but are critical for the stability of the late intermediate, L, and the M-state. Alanine substitution of hydrophobic residues at more peripheral helix-helix contact sites of the native structure, which are still absent or unstable in the M-state, shows both positive (destabilizing) and negative (stabilizing) ΔΔ G, indicating that non-native contacts are formed initially and weakened or lost as a result of subsequent structural rearrangement steps.

Indexed as

AnimalsApoproteinsHydrogen-Ion ConcentrationHydrophobic and Hydrophilic InteractionsKineticsMutagenesis, Site-DirectedMutationMyoglobinProtein Conformation, alpha-HelicalProtein UnfoldingSperm WhaleThermodynamicsapomyoglobinApoproteinsMyoglobin

Identifiers

PMID30133301
PMCPMC6395567

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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.