Evidence map›Paper›PMID 29806025›Full record

ArticleScience advances2018

Gold nanocrystal labels provide a sequence-to-3D structure map in SAXS reconstructions.

Thomas Zettl, Rebecca S Mathew, Xuesong Shi, Sebastian Doniach, Daniel Herschlag, Pehr A B Harbury, Jan Lipfert

Open access · goldAbstract read
In one paragraph

Article in Science advances, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.7field-weighted citation impact, top 35% of its field
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

4 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Site-specific covalent labeling of large RNAs with nanoparticles empowered by expanded genetic alphabet transcription.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  3. Article
  4. 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

7 authors at 3 institutions in 2 countries.

Thomas ZettlDepartment of Physics, Nanosystems Initiative Munich, and Center for Nanoscience, LMU Munich, Munich, Germany.ORCID 0000-0003-2963-1589
Rebecca S MathewDepartment of Cell Biology, Harvard Medical School, Harvard University, Boston, MA 02115, USA.ORCID 0000-0001-7187-4870
Xuesong ShiDepartment of Biochemistry, Stanford University, Stanford, CA 94305, USA.
Sebastian DoniachDepartments of Applied Physics and Physics, Stanford University, Stanford, CA 94305, USA.ORCID 0000-0001-5948-5821
Daniel HerschlagDepartment of Biochemistry, Stanford University, Stanford, CA 94305, USA.
Pehr A B HarburyDepartment of Biochemistry, Stanford University, Stanford, CA 94305, USA.ORCID 0000-0002-3657-5485
Jan LipfertDepartment of Physics, Nanosystems Initiative Munich, and Center for Nanoscience, LMU Munich, Munich, Germany.ORCID 0000-0003-3613-7896
Stanford University · USNanosystems Initiative Munich · DEHarvard University · US

Funding

Time-resolved small angle X-ray scatteringP01GM066275 · NIGMS · STANFORD UNIVERSITY · PI HERSCHLAG, DANIEL · 2003 to 2017
$17.8M
NIGMS NIH HHS P01 GM066275
6 · The paper itself

Abstract

Small-angle x-ray scattering (SAXS) is a powerful technique to probe the structure of biological macromolecules and their complexes under virtually arbitrary solution conditions, without the need for crystallization. While it is possible to reconstruct molecular shapes from SAXS data ab initio, the resulting electron density maps have a resolution of ~1 nm and are often insufficient to reliably assign secondary structure elements or domains. We show that SAXS data of gold-labeled samples significantly enhance the information content of SAXS measurements, allowing the unambiguous assignment of macromolecular sequence motifs to specific locations within a SAXS structure. We first demonstrate our approach for site-specifically internally and end-labeled DNA and an RNA motif. In addition, we present a protocol for highly uniform and site-specific labeling of proteins with small (~1.4 nm diameter) gold particles and apply our method to the signaling protein calmodulin. In all cases, the position of the small gold probes can be reliably identified in low-resolution electron density maps. Enhancing low-resolution measurements by site-selective gold labeling provides an attractive approach to aid modeling of a large range of macromolecular systems.

Indexed as

GoldMolecular ConformationNanoparticlesScattering, Small AngleX-Ray DiffractionAlgorithmsBase SequenceDNAModels, MolecularProteinsDNAGoldProteins

Identifiers

PMID29806025
PMCPMC5969820
OpenAlexW2803512730

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

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.