Evidence map›Paper›PMID 23760106›Full record

ArticleLab on a chip2013

A simple three-dimensional-focusing, continuous-flow mixer for the study of fast protein dynamics.

Kelly S Burke, Dzmitry Parul, Michael J Reddish, R Brian Dyer

Abstract read
In one paragraph

Article in Lab on a chip, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.0field-weighted citation impact, top 23% 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

9 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Review
  6. Sandwich-format 3D printed microfluidic mixers: a flexible platform for multi-probe analysis.Journal of micromechanics and microengineering : structures, devices, and systems · 2015
    Article
  7. Article
  8. Review
  9. 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

4 authors at 2 institutions in 1 country.

Kelly S BurkeDivision of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, California 91106, USA.
Dzmitry Parul
Michael J Reddish
R Brian Dyer
Emory University · USCalifornia Institute of Technology · US

Funding

Proton Transfer Dynamics in Heme-Copper OxidasesP01GM068036 · NIGMS · ALBERT EINSTEIN COL OF MED YESHIVA UNIV · PI CALLENDER, ROBERT · 2004 to 2018
$26.4M
EARLY EVENTS IN PROTEIN FOLDINGR01GM053640 · NIGMS · UNIVERSITY OF CALIF-LOS ALAMOS NAT LAB · PI DYER, RICHARD BRIAN · 1996 to 2022
$6.5M
NIGMS NIH HHS GM053640NIGMS NIH HHS GM068036NIGMS NIH HHS P01 GM068036NIGMS NIH HHS R01 GM053640
6 · The paper itself

Abstract

We present a simple, yet flexible microfluidic mixer with a demonstrated mixing time as short as 80 μs that is widely accessible because it is made of commercially available parts. To simplify the study of fast protein dynamics, we have developed an inexpensive continuous-flow microfluidic mixer, requiring no specialized equipment or techniques. The mixer uses three-dimensional, hydrodynamic focusing of a protein sample stream by a surrounding sheath solution to achieve rapid diffusional mixing between the sample and sheath. Mixing initiates the reaction of interest. Reactions can be spatially observed by fluorescence or absorbance spectroscopy. We characterized the pixel-to-time calibration and diffusional mixing experimentally. We achieved a mixing time as short as 80 μs. We studied the kinetics of horse apomyoglobin (apoMb) unfolding from the intermediate (I) state to its completely unfolded (U) state, induced by a pH jump from the initial pH of 4.5 in the sample stream to a final pH of 2.0 in the sheath solution. The reaction time was probed using the fluorescence of 1-anilinonaphthalene-8-sulfonate (1,8-ANS) bound to the folded protein. We observed unfolding of apoMb within 760 μs, without populating additional intermediate states under these conditions. We also studied the reaction kinetics of the conversion of pyruvate to lactate catalyzed by lactate dehydrogenase using the intrinsic tryptophan emission of the enzyme. We observe sub-millisecond kinetics that we attribute to Michaelis complex formation and loop domain closure. These results demonstrate the utility of the three-dimensional focusing mixer for biophysical studies of protein dynamics.

Indexed as

Protein UnfoldingAnilino NaphthalenesulfonatesAnimalsApoproteinsEnzyme AssaysEquipment DesignFluorescent DyesHorsesKineticsLactic AcidL-Lactate DehydrogenaseMicrofluidic Analytical TechniquesMyoglobinPyruvic AcidSwine8-anilino-1-naphthalenesulfonic acidAnilino NaphthalenesulfonatesapomyoglobinApoproteinsFluorescent DyesLactic AcidL-Lactate DehydrogenaseMyoglobinPyruvic Acid

Identifiers

PMID23760106
PMCPMC3733270
OpenAlexW2092089910

What OpenQuestion holds

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LicenceTDM
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.