Evidence map›Paper›PMID 27886066›Full record

ArticleInternational journal of molecular sciences2016

Importance of Heat and Pressure for Solubilization of Recombinant Spider Silk Proteins in Aqueous Solution.

Justin A Jones, Thomas I Harris, Paula F Oliveira, Brianne E Bell, Abdulrahman Alhabib, Randolph V Lewis

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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.

Justin A JonesDepartment of Biology, Utah State University, Logan, UT 84341, USA. justin.a.jones@usu.edu.
Thomas I HarrisDepartment of Biological Engineering, Utah State University, Logan, UT 84341, USA. tiharristh@gmail.com.
Paula F OliveiraDepartment of Biology, Utah State University, Logan, UT 84341, USA. paula.oliveira@usu.edu.
Brianne E BellDepartment of Biology, Utah State University, Logan, UT 84341, USA. brianne.bell@aggiemail.usu.edu.
Abdulrahman AlhabibDepartment of Biology, Utah State University, Logan, UT 84341, USA. abood.alhabib@hotmail.com.
Randolph V LewisDepartment of Biology, Utah State University, Logan, UT 84341, USA. randy.lewis@usu.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The production of recombinant spider silk proteins continues to be a key area of interest for a number of research groups. Several key obstacles exist in their production as well as in their formulation into useable products. The original reported method to solubilize recombinant spider silk proteins (rSSp) in an aqueous solution involved using microwaves to quickly generate heat and pressure inside of a sealed vial containing rSSp and water. Fibers produced from this system are remarkable in their mechanical ability and demonstrate the ability to be stretched and recover 100 times. The microwave method dissolves the rSSPs with dissolution time increasing with higher molecular weight constructs, increasing concentration of rSSPs, protein type, and salt concentration. It has proven successful in solvating a number of different rSSPs including native-like sequences (MaSp1, MaSp2, piriform, and aggregate) as well as chimeric sequences (FlAS) in varied concentrations that have been spun into fibers and formed into films, foams, sponges, gels, coatings, macro and micro spheres and adhesives. The system is effective but inherently unpredictable and difficult to control. Provided that the materials that can be generated from this method of dissolution are impressive, an alternative means of applying heat and pressure that is controllable and predictable has been developed. Results indicate that there are combinations of heat and pressure (135 °C and 140 psi) that result in maximal dissolution without degrading the recombinant MaSp2 protein tested, and that heat and pressure are the key elements to the method of dissolution.

Indexed as

Hot TemperaturePressureAmino Acid SequenceAnimalsBase SequenceCloning, MolecularEscherichia coliFibroinsGene ExpressionGoatsMaterials TestingMicrowavesRecombinant ProteinsSolubilitySolutionsSpidersFibroinsRecombinant ProteinsSolutionsWateraqueousfibersheatpressurerecombinant spider silk proteinssolvation

Identifiers

PMID27886066
PMCPMC5133949

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.