Evidence map›Paper›PMID 24889060›Full record

ArticleAngewandte Chemie (International ed. in English)2014

Measuring fate and rate of single-molecule competition of amplification and restriction digestion, and its use for rapid genotyping tested with hepatitis C viral RNA.

Bing Sun, Jesus Rodriguez-Manzano, David A Selck, Eugenia Khorosheva, Mikhail A Karymov, Rustem F Ismagilov

Abstract read
In one paragraph

Article in Angewandte Chemie (International ed. in English), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

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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

6 authors.

Bing Sun *Division of Chemistry and Chemical Engineering California Institute of Technology 1200 E. California Blvd. Pasadena, CA 91125 (USA).
Jesus Rodriguez-Manzano *Division of Chemistry and Chemical Engineering California Institute of Technology 1200 E. California Blvd. Pasadena, CA 91125 (USA).
David A SelckDivision of Chemistry and Chemical Engineering California Institute of Technology 1200 E. California Blvd. Pasadena, CA 91125 (USA).
Eugenia KhoroshevaDivision of Chemistry and Chemical Engineering California Institute of Technology 1200 E. California Blvd. Pasadena, CA 91125 (USA).
Mikhail A KarymovDivision of Chemistry and Chemical Engineering California Institute of Technology 1200 E. California Blvd. Pasadena, CA 91125 (USA).
Rustem F IsmagilovDivision of Chemistry and Chemical Engineering California Institute of Technology 1200 E. California Blvd. Pasadena, CA 91125 (USA).

Funding

PREDOCTORAL TRAINING IN BIOLOGY AND CHEMISTRYT32GM007616 · NIGMS · CALIFORNIA INSTITUTE OF TECHNOLOGY · PI STERNBERG, PAUL WARREN · 1985 to 2019
$22.9M
2007 NIH Director's Pioneer Award Program (DP1)DP1OD003584 · OD · UNIVERSITY OF CHICAGO · PI ISMAGILOV, RUSTEM F · 2007 to 2011
$3.9M
Digital SlipChip Technology for POC and Resource-Limited Viral Load MeasurementsR01EB012946 · NIBIB · UNIVERSITY OF CHICAGO · PI ISMAGILOV, RUSTEM F · 2011 to 2014
$2.0M
New Microfluidic Technology as Research Tool for BiologyR01EB001903 · NIBIB · UNIVERSITY OF CHICAGO · PI ISMAGILOV, RUSTEM F · 2003 to 2007
$1.6M
NIBIB NIH HHS R01 EB001903NIBIB NIH HHS R01 EB012946NIBIB NIH HHS R01EB012946NIGMS NIH HHS 5T32GM07616NIGMS NIH HHS T32 GM007616NIH HHS DP1 OD003584NIH HHS DP1OD003584
6 · The paper itself

Abstract

We experimentally monitored, at the single-molecule level, the competition among reverse transcription, exponential amplification (RT-LAMP), and linear degradation (restriction enzymes) starting with hepatitis C viral RNA molecules. We found significant heterogeneity in the rate of single-molecule amplification; introduction of the restriction enzymes affected both the rate and the "fate" (the binary outcome) of single-molecule amplification. While end-point digital measurements were primarily sensitive to changes in fate, the bulk real-time kinetic measurements were dominated by the rate of amplification of the earliest molecules, and were not sensitive to fate of the rest of the molecules. We show how this competition of reactions can be used for rapid HCV genotyping with either digital or bulk readout. This work advances our understanding of single-molecule dynamics in reaction networks and may help bring genotyping capabilities out of clinical labs and into limited-resource settings.

Indexed as

GenotypeHepacivirusRNA, ViralRNA, Viralanalytical methodsgenotypingglobal healthhepatitis Csingle-molecule studies

Identifiers

PMID24889060
PMCPMC4116457

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.