Evidence map›Paper›PMID 29017728›Full record

ArticleBiophysical journal2017

Near-Infrared Fluorescent Proteins Engineered from Bacterial Phytochromes in Neuroimaging.

Kiryl D Piatkevich, Ho-Jun Suk, Suhasa B Kodandaramaiah, Fumiaki Yoshida, Ellen M DeGennaro, Mikhail Drobizhev, Thomas E Hughes, Robert Desimone, Edward S Boyden, Vladislav V Verkhusha

Abstract read
In one paragraph

Article in Biophysical journal, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

33 citing papers in PubMed, 58 citations in OpenAlex.

  1. Article
  2. OPTRACE: Optical Imaging-Guided Transplantation and Tracking of Cells in the Mouse Brain.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
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  15. Rapid directed molecular evolution of fluorescent proteins in mammalian cells.Protein science : a publication of the Protein Society · 2022
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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

10 authors at 4 institutions in 1 country.

Kiryl D PiatkevichMedia Lab, MIT, Cambridge, Massachusetts; MIT McGovern Institute for Brain Research, MIT, Cambridge, Massachusetts.
Ho-Jun SukMedia Lab, MIT, Cambridge, Massachusetts; Harvard-MIT Division of Health Sciences and Technology, MIT, Cambridge, Massachusetts.
Suhasa B KodandaramaiahMedia Lab, MIT, Cambridge, Massachusetts; MIT McGovern Institute for Brain Research, MIT, Cambridge, Massachusetts.
Fumiaki YoshidaMIT McGovern Institute for Brain Research, MIT, Cambridge, Massachusetts.
Ellen M DeGennaroMIT McGovern Institute for Brain Research, MIT, Cambridge, Massachusetts; Department of Brain and Cognitive Sciences, MIT, Cambridge, Massachusetts.
Mikhail DrobizhevDepartment of Cell Biology and Neuroscience, Montana State University, Bozeman, Montana.
Thomas E HughesDepartment of Cell Biology and Neuroscience, Montana State University, Bozeman, Montana.
Robert DesimoneMIT McGovern Institute for Brain Research, MIT, Cambridge, Massachusetts; Department of Brain and Cognitive Sciences, MIT, Cambridge, Massachusetts.
Edward S BoydenMedia Lab, MIT, Cambridge, Massachusetts; MIT McGovern Institute for Brain Research, MIT, Cambridge, Massachusetts; Department of Brain and Cognitive Sciences, MIT, Cambridge, Massachusetts; Department of Biological Engineering, MIT, Cambridge, Massachusetts; MIT Center for Neurobiological Engineering, MIT, Cambridge, Massachusetts. Electronic address: esb@media.mit.edu.
Vladislav V VerkhushaDepartment of Anatomy and Structural Biology, Albert Einstein College of Medicine, Bronx, New York; Gruss-Lipper Biophotonics Center, Albert Einstein College of Medicine, Bronx, New York. Electronic address: vladislav.verkhusha@einstein.yu.edu.
McGovern Institute for Brain Research · USMontana State University · USAlbert Einstein College of Medicine · USHarvard–MIT Division of Health Sciences and Technology · US

Funding

Novel Platforms for Systematic Optical Control of Complex Neural Circuits In VivoR01DA029639 · NIDA · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI BOYDEN, EDWARD S. · 2010 to 2023
$6.7M
Redesigning General Anesthesia (Admin Supp)R01GM104948 · NIGMS · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI BOYDEN, EDWARD S., BROWN, EMERY N · 2012 to 2016
$4.4M
Near-Infrared Fluorescent Proteins, Biosensors and Optogenetic ToolsR35GM122567 · NIGMS · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI Vladislav Verkhusha · 2017 to 2026
$4.3M
High-throughput robotic analysis of integrated neuronal phenotypesR01EY023173 · NEI · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI BOYDEN, EDWARD S., FOREST, CRAIG · 2012 to 2016
$4.3M
Near Infrared Genetically Encoded Voltage Indicators (NIR-GEVIs) for All-Optical Electrophysiology (AOE)U01NS099573 · NINDS · IMPERIAL COLLEGE OF SCIENCE, TECHNOLOGY AND MEDICINE · PI ANTIC, SRDJAN D, KNOPFEL, THOMAS · 2016 to 2018
$2.9M
Resource for Multiphoton Characterization of Genetically-Encoded ProbesU24NS109107 · NINDS · MONTANA STATE UNIVERSITY - BOZEMAN · PI Mikhail Drobizhev · 2018 to 2026
$2.2M
Northern Lights collaboration for better 2-photon probesU01NS094246 · NINDS · MONTANA STATE UNIVERSITY - BOZEMAN · PI CAMPBELL, ROBERT E., DROBIZHEV, MIKHAIL · 2015 to 2017
$2.0M
Calcium biosensors for deep-tissue imaging and spectral multiplexingU01NS103573 · NINDS · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI VERKHUSHA, VLADISLAV · 2017 to 2019
$1.8M
NEI NIH HHS R01 EY023173NIDA NIH HHS R01 DA029639NIGMS NIH HHS R01 GM104948NIGMS NIH HHS R35 GM122567NINDS NIH HHS U01 NS094246NINDS NIH HHS U01 NS099573NINDS NIH HHS U01 NS103573NINDS NIH HHS U24 NS109107
6 · The paper itself

Abstract

Several series of near-infrared (NIR) fluorescent proteins (FPs) were recently engineered from bacterial phytochromes but were not systematically compared in neurons. To fluoresce, NIR FPs utilize an enzymatic derivative of heme, the linear tetrapyrrole biliverdin, as a chromophore whose level in neurons is poorly studied. Here, we evaluated NIR FPs of the iRFP protein family, which were reported to be the brightest in non-neuronal mammalian cells, in primary neuronal culture, in brain slices of mouse and monkey, and in mouse brain in vivo. We applied several fluorescence imaging modes, such as wide-field and confocal one-photon and two-photon microscopy, to compare photochemical and biophysical properties of various iRFPs. The iRFP682 and iRFP670 proteins exhibited the highest brightness and photostability under one-photon and two-photon excitation modes, respectively. All studied iRFPs exhibited efficient binding of the endogenous biliverdin chromophore in cultured neurons and in the mammalian brain and can be readily applied to neuroimaging.

Indexed as

Infrared RaysNeuroimagingAnimalsLuminescent ProteinsMacaca mulattaMaleMiceMicroscopy, FluorescenceNeuronsPhytochromeProtein EngineeringLuminescent ProteinsPhytochrome

Identifiers

PMID29017728
PMCPMC5700256
OpenAlexW2763161598

What OpenQuestion holds

Textmetadata
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.