Evidence map›Paper›PMID 26921961›Full record

ArticleMethods in enzymology2016

Production of Recombinant Chemokines and Validation of Refolding.

Christopher T Veldkamp, Chad A Koplinski, Davin R Jensen, Francis C Peterson, Kaitlin M Smits, Brittney L Smith, Scott K Johnson, Christina Lettieri, Wallace G Buchholz, Joyce C Solheim and 1 more

Abstract read
In one paragraph

Article in Methods in enzymology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
8.4field-weighted citation impact, top 3% 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

27 citing papers in PubMed, 41 citations in OpenAlex.

  1. Article
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  3. The N-terminal ELRThe Journal of biological chemistry · 2025
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  10. AnInternational journal of molecular sciences · 2022
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  20. Fluorescently Tagged CCL19 and CCL21 to Monitor CCR7 and ACKR4 Functions.International journal of molecular sciences · 2018
    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

11 authors at 4 institutions in 1 country.

Christopher T VeldkampDepartment of Biochemistry, Medical College of Wisconsin, Milwaukee, Wisconsin, USA; Department of Chemistry, University of Wisconsin-Whitewater, Whitewater, Wisconsin, USA. Electronic address: veldkamc@uww.edu.
Chad A KoplinskiDepartment of Biochemistry, Medical College of Wisconsin, Milwaukee, Wisconsin, USA.
Davin R JensenDepartment of Biochemistry, Medical College of Wisconsin, Milwaukee, Wisconsin, USA.
Francis C PetersonDepartment of Biochemistry, Medical College of Wisconsin, Milwaukee, Wisconsin, USA.
Kaitlin M SmitsDepartment of Biochemistry and Molecular Biology, University of Nebraska Medical Center, Omaha, Nebraska, USA; Department of Pathology and Microbiology, University of Nebraska Medical Center, Omaha, Nebraska, USA; The Eppley Institute and the Fred and Pamela Buffett Cancer Center, University of Nebraska Medical Center, Omaha, Nebraska, USA.
Brittney L SmithDepartment of Biochemistry and Molecular Biology, University of Nebraska Medical Center, Omaha, Nebraska, USA; Department of Pathology and Microbiology, University of Nebraska Medical Center, Omaha, Nebraska, USA; The Eppley Institute and the Fred and Pamela Buffett Cancer Center, University of Nebraska Medical Center, Omaha, Nebraska, USA.
Scott K JohnsonBiological Process Development Facility, College of Engineering, University of Nebraska-Lincoln, Lincoln, Nebraska, USA.
Christina LettieriDepartment of Pediatrics, Children's Hospital and Medical Center, University of Nebraska Medical Center, Omaha, Nebraska, USA.
Wallace G BuchholzBiological Process Development Facility, College of Engineering, University of Nebraska-Lincoln, Lincoln, Nebraska, USA.
Joyce C SolheimDepartment of Biochemistry and Molecular Biology, University of Nebraska Medical Center, Omaha, Nebraska, USA; Department of Pathology and Microbiology, University of Nebraska Medical Center, Omaha, Nebraska, USA; The Eppley Institute and the Fred and Pamela Buffett Cancer Center, University of Nebraska Medical Center, Omaha, Nebraska, USA.
Brian F VolkmanDepartment of Biochemistry, Medical College of Wisconsin, Milwaukee, Wisconsin, USA.
Medical College of Wisconsin · USUniversity of Nebraska Medical Center · USUniversity of Nebraska–Lincoln · USUniversity of Wisconsin–Whitewater · US

Funding

UNMC/EPPLEY CANCER CENTER SUPPORT GRANTP30CA036727 · NCI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI Apar Kishor Ganti · 1985 to 2026
$55.0M
Tissue CoreP50CA127297 · NCI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI HOLLINGSWORTH, MICHAEL A. · 2008 to 2018
$17.1M
Structural Basis for Chemokine FunctionR01AI058072 · NIAID · MEDICAL COLLEGE OF WISCONSIN · PI VOLKMAN, BRIAN F · 2004 to 2019
$4.1M
Sulfotyrosine-guided discovery of small molecule chemokine inhibitorsR01GM097381 · NIGMS · MEDICAL COLLEGE OF WISCONSIN · PI VOLKMAN, BRIAN F · 2011 to 2021
$2.9M
Structural Basis for Chemokine FunctionR37AI058072 · NIAID · MEDICAL COLLEGE OF WISCONSIN · PI Brian F Volkman · 2020 to 2026
$2.8M
Function and Targeting of CCR6/CCL20 in Autoimmune Psoriasiform Skin DiseaseR01AR063091 · NIAMS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI HWANG, SAM T · 2013 to 2017
$1.6M
Structural studies of chemokines that target metastatic cancer cells to the lymphR15CA159202 · NCI · UNIVERSITY OF WISCONSIN WHITEWATER · PI VELDKAMP, CHRISTOPHER T · 2011 to 2011
$335k
Flt3L Treatment of Pancreatic CancerR03CA173223 · NCI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI SOLHEIM, JOYCE C · 2013 to 2014
$146k
ATTENUATION CONTROL OF GENE EXPRESSION IN BACTERIAR01GM009738 · NIGMS · STANFORD UNIVERSITY · PI YANOFSKY, CHARLES · 1985 to 1988
–
NCI NIH HHS 1R15CA159202-01NCI NIH HHS P30 CA036727NCI NIH HHS P30CA036727NCI NIH HHS P50 CA127297NCI NIH HHS P50CA127297NCI NIH HHS R03 CA173223NCI NIH HHS R03CA173223NCI NIH HHS R15 CA159202NIAID NIH HHS R01 AI058072NIAID NIH HHS R01AI058072NIAID NIH HHS R37 AI058072NIAMS NIH HHS R01 AR063091NIGMS NIH HHS R01GM09738NIGMS NIH HHS R01 GM097381
6 · The paper itself

Abstract

The diverse roles of chemokines in normal immune function and many human diseases have motivated numerous investigations into the structure and function of this family of proteins. Recombinant chemokines are often used to study how chemokines coordinate the trafficking of immune cells in various biological contexts. A reliable source of biologically active protein is vital for any in vitro or in vivo functional analysis. In this chapter, we describe a general method for the production of recombinant chemokines and robust techniques for efficient refolding that ensure consistently high biological activity. Considerations for initiating development of protocols consistent with Current Good Manufacturing Practices (cGMPs) to produce biologically active chemokines suitable for use in clinical trials are also discussed.

Indexed as

ChemotaxisChromatography, AffinityChromatography, High Pressure LiquidCyclic GMPDisulfidesEscherichia coliNuclear Magnetic Resonance, BiomolecularProtein EngineeringProtein Processing, Post-TranslationalProtein RefoldingRecombinant ProteinsReproducibility of ResultsCyclic GMPDisulfidesRecombinant ProteinscGMPChemokineChemokine oxidationChemokine purificationChemokine refoldingExpressionMass spectrometryMass spectrometry of chemokinesNMRProteinProtein foldingProtein NMRPurificationRecombinant chemokinesRecombinant cytokinesRefolding

Identifiers

PMID26921961
PMCPMC4811038
OpenAlexW2179993597

What OpenQuestion holds

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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.