Evidence map›Paper›PMID 22325262›Full record

ArticleBiophysical journal2012

A hot-spot motif characterizes the interface between a designed ankyrin-repeat protein and its target ligand.

Luthur Siu-Lun Cheung, Manu Kanwar, Marc Ostermeier, Konstantinos Konstantopoulos

Abstract read
In one paragraph

Article in Biophysical journal, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Molecular Docking and Molecular Dynamics Simulations in Related toTropical medicine and infectious disease · 2023
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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

4 authors.

Luthur Siu-Lun CheungDepartment of Chemical and Biomolecular Engineering, The Johns Hopkins University, Baltimore, Maryland, USA.
Manu Kanwar
Marc Ostermeier
Konstantinos Konstantopoulos

Funding

The Combinatorial Design of Protein Molecular SwitchesR01GM066972 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI OSTERMEIER, MARC A · 2003 to 2016
$4.0M
Molecular Characterization of Cell-Cell Interactions in Cancer MetastasisR01CA101135 · NCI · JOHNS HOPKINS UNIVERSITY · PI KONSTANTOPOULOS, KONSTANTINOS · 2003 to 2011
$2.5M
NCI NIH HHS R01 CA101135NIGMS NIH HHS R01 GM066972NIGMS NIH HHS R01-GM066972
6 · The paper itself

Abstract

Nonantibody scaffolds such as designed ankyrin repeat proteins (DARPins) can be rapidly engineered to detect diverse target proteins with high specificity and offer an attractive alternative to antibodies. Using molecular simulations, we predicted that the binding interface between DARPin off7 and its ligand (maltose binding protein; MBP) is characterized by a hot-spot motif in which binding energy is largely concentrated on a few amino acids. To experimentally test this prediction, we fused MBP to a transmembrane domain to properly orient the protein into a polymer-cushioned lipid bilayer, and characterized its interaction with off7 using force spectroscopy. Using this, to our knowledge, novel technique along with surface plasmon resonance, we validated the simulation predictions and characterized the effects of select mutations on the kinetics of the off7-MBP interaction. Our integrated approach offers scientific insights on how the engineered protein interacts with the target molecule.

Indexed as

Ankyrin RepeatMolecular Dynamics SimulationProtein EngineeringAmino Acid MotifsAmino Acid SequenceKineticsLigandsLipid BilayersMaltose-Binding ProteinsMolecular Sequence DataMutationProtein BindingSpectrum AnalysisSurface Plasmon ResonanceThermodynamicsLigandsLipid BilayersMaltose-Binding Proteins

Identifiers

PMID22325262
PMCPMC3274810

What OpenQuestion holds

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Registered trials

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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.