Evidence map›Paper›PMID 37379021›Full record

ArticleAdvanced healthcare materials2023

Moderate-Affinity Affibodies Modulate the Delivery and Bioactivity of Bone Morphogenetic Protein-2.

Jonathan Dorogin, Henry B Hochstatter, Samantha O Shepherd, Justin E Svendsen, Morrhyssey A Benz, Andrew C Powers, Karly M Fear, Jakob M Townsend, James S Prell, Parisa Hosseinzadeh and 1 more

Open access · hybridAbstract read
In one paragraph

Article in Advanced healthcare materials, 2023. 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
3.1field-weighted citation impact, top 9% 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

12 citing papers in PubMed, 15 citations in OpenAlex.

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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

11 authors at 1 institution in 1 country.

Jonathan DoroginDepartment of Bioengineering, Knight Campus for Accelerating Scientific Impact, University of Oregon, 6231 University of Oregon, Eugene, OR, 97403, USA.ORCID 0000-0003-4694-1415
Henry B HochstatterDepartment of Bioengineering, Knight Campus for Accelerating Scientific Impact, University of Oregon, 6231 University of Oregon, Eugene, OR, 97403, USA.
Samantha O ShepherdDepartment of Chemistry and Biochemistry, University of Oregon, 1253 University of Oregon, Eugene, OR, 97403, USA.
Justin E SvendsenDepartment of Bioengineering, Knight Campus for Accelerating Scientific Impact, University of Oregon, 6231 University of Oregon, Eugene, OR, 97403, USA.
Morrhyssey A BenzDepartment of Bioengineering, Knight Campus for Accelerating Scientific Impact, University of Oregon, 6231 University of Oregon, Eugene, OR, 97403, USA.
Andrew C PowersDepartment of Bioengineering, Knight Campus for Accelerating Scientific Impact, University of Oregon, 6231 University of Oregon, Eugene, OR, 97403, USA.
Karly M FearDepartment of Bioengineering, Knight Campus for Accelerating Scientific Impact, University of Oregon, 6231 University of Oregon, Eugene, OR, 97403, USA.
Jakob M TownsendDepartment of Bioengineering, Knight Campus for Accelerating Scientific Impact, University of Oregon, 6231 University of Oregon, Eugene, OR, 97403, USA.
James S PrellDepartment of Chemistry and Biochemistry, University of Oregon, 1253 University of Oregon, Eugene, OR, 97403, USA.
Parisa HosseinzadehDepartment of Bioengineering, Knight Campus for Accelerating Scientific Impact, University of Oregon, 6231 University of Oregon, Eugene, OR, 97403, USA.
Marian H HettiaratchiDepartment of Bioengineering, Knight Campus for Accelerating Scientific Impact, University of Oregon, 6231 University of Oregon, Eugene, OR, 97403, USA.ORCID 0000-0001-8187-4575
University of Oregon · US

Funding

Modulating Protein Activity in Tissue Repair using Engineered Affinity-based BiomaterialsR35GM147507 · NIGMS · UNIVERSITY OF OREGON · PI Marian Hirushika Hettiaratchi · 2022 to 2026
$2.0M
A Directed Evolution Approach to Affinity-Based Protein DeliveryR21EB032112 · NIBIB · UNIVERSITY OF OREGON · PI HETTIARATCHI, MARIAN HIRUSHIKA · 2021 to 2023
$602k
NIBIB NIH HHS R21 EB032112NIGMS NIH HHS R35 GM147507
6 · The paper itself

Abstract

Uncontrolled bone morphogenetic protein-2 (BMP-2) release can lead to off-target bone growth and other adverse events. To tackle this challenge, yeast surface display is used to identify unique BMP-2-specific protein binders known as affibodies that bind to BMP-2 with different affinities. Biolayer interferometry reveals an equilibrium dissociation constant of 10.7 nm for the interaction between BMP-2 and high-affinity affibody and 34.8 nm for the interaction between BMP-2 and the low-affinity affibody. The low-affinity affibody-BMP-2 interaction also exhibits an off-rate constant that is an order of magnitude higher. Computational modeling of affibody-BMP-2 binding predicts that the high- and low-affinity affibodies bind to two distinct sites on BMP-2 that function as different cell-receptor binding sites. BMP-2 binding to affibodies reduces expression of the osteogenic marker alkaline phosphatase (ALP) in C2C12 myoblasts. Affibody-conjugated polyethylene glycol-maleimide hydrogels increase uptake of BMP-2 compared to affibody-free hydrogels, and high-affinity hydrogels exhibit lower BMP-2 release into serum compared to low-affinity hydrogels and affibody-free hydrogels over four weeks. Loading BMP-2 into affibody-conjugated hydrogels prolongs ALP activity of C2C12 myoblasts compared to soluble BMP-2. This work demonstrates that affibodies with different affinities can modulate BMP-2 delivery and activity, creating a promising approach for controlling BMP-2 delivery in clinical applications.

Indexed as

Biocompatible MaterialsBone Morphogenetic Protein 2HydrogelsMyoblastsOsteogenesisSignal TransductionBiocompatible MaterialsBone Morphogenetic Protein 2Hydrogelsaffibodiesbone morphogenetic protein-2controlled protein deliveryhydrogels

Identifiers

PMID37379021
PMCPMC10592408
OpenAlexW4382343789

What OpenQuestion holds

Textmetadata
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.