Evidence map›Paper›PMID 41614783›Full record

ReviewCurrent issues in molecular biology2025

Differences and Similarities in Protein and Nucleic Acid Structures and Their Biological Interactions.

Tsutomu Arakawa, Taiji Oyama, Tomoto Ura, Suguru Nishinami, Kentaro Shiraki, Teruo Akuta

Abstract readReview
In one paragraph

Review in Current issues in molecular biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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.

Tsutomu ArakawaAlliance Protein Laboratories, 13380 Pantera Road, San Diego, CA 92130, USA.
Taiji OyamaSales Division, JASCO Corporation, 2967-5 Ishikawa, Hachioji 192-8537, Japan.ORCID 0000-0003-1403-073X
Tomoto UraInstitute of Pure and Applied Sciences, University of Tsukuba, Tsukuba 305-8573, Japan.ORCID 0000-0001-9644-1078
Suguru NishinamiInstitute for Genetic Medicine, Hokkaido University, Sapporo 060-0815, Japan.ORCID 0009-0005-7534-4881
Kentaro ShirakiInstitute of Pure and Applied Sciences, University of Tsukuba, Tsukuba 305-8573, Japan.
Teruo AkutaResearch and Development Division, Kyokuto Pharmaceutical Industrial Co., Ltd., 3333-26, Aza-Asayama, Kamitezuna, Tahahagi 318-004, Japan.ORCID 0000-0002-0669-4379

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Protein and nucleic acid play central roles in biology and pharmaceuticals. Both share a similar architecture made of a backbone and side chains. Protein has a peptide backbone and various side chains, whereas nucleic acid has a phosphate backbone and aromatic side chains. However, they are significantly different in the chemical properties of the backbone and side chains. The protein backbone is uncharged, while nucleic acid backbone is negatively charged. The protein side chains comprise widely different chemical properties. On the other hand, the nucleic acid side chains comprise a uniform chemical property of aromatic bases. Such differences lead to fundamentally different folding, molecular interactions and co-solvent interactions, which are the focus of this review. In regular protein secondary structures, the peptide groups form polar hydrogen bonds, making the interior hydrophilic. The side chains of different chemical properties are exposed on the outside of the protein secondary structures and participate in molecular and co-solvent interactions. On the other hand, hydrophobic/aromatic nucleobase side chains are located inside the typical double helix or quadruplex structures. The charged phosphate groups of the nucleic acid backbone are located outside, participating in electrostatic interactions. The nucleobases are also involved in molecular interactions, when exposed in breaks, hairpins, kinks and loops. These structural differences between protein and nucleic acid confer different interactions with commonly used co-solvents, such as denaturants, organic solvents and polymers.

Indexed as

aromatic side chainmolecular interactionspeptide backbonephosphate backbonesecondary structureside chain

Identifiers

PMID41614783
PMCPMC12731849

What OpenQuestion holds

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Registered trials

None linked

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.