Evidence map›Paper›PMID 21601097›Full record

ArticleMethods in enzymology2011

Synthetic physiology strategies for adapting tools from nature for genetically targeted control of fast biological processes.

Brian Y Chow, Amy S Chuong, Nathan C Klapoetke, Edward S Boyden

Open access · greenAbstract read
In one paragraph

Article in Methods in enzymology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
3.9field-weighted citation impact, top 6% 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

7 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
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  5. Review
  6. Review
  7. Diversity of Chlamydomonas channelrhodopsins.Photochemistry and photobiology
    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

4 authors at 2 institutions in 1 country.

Brian Y ChowSynthetic Neurobiology Group, The Media Laboratory and McGovern Institute, Departments of Biological Engineering and Brain and Cognitive Sciences, Massachusetts Institute of Technology, Cambridge, Massachusetts, USA.
Amy S Chuong
Nathan C Klapoetke
Edward S Boyden
Massachusetts Institute of Technology · USMcGovern Institute for Brain Research · 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
Novel Tools and Principles for Precisely Controlling Brain ActivityDP2OD002002 · OD · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI BOYDEN, EDWARD S. · 2007 to 2007
$2.5M
CRCNS: Gamma Rhythms and Cell AssembliesR01NS067199 · NINDS · BOSTON UNIVERSITY (CHARLES RIVER CAMPUS) · PI KOPELL, NANCY · 2009 to 2013
$1.7M
Modulating Cortical and Sub-cortical Brain Circuits in Chronic Facial PainRC2DE020919 · NIDCR · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI BOYDEN, EDWARD S. · 2009 to 2010
$994k
Optogenetic control of attention through prefrontal synchronyRC1MH088182 · NIMH · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI DESIMONE, ROBERT · 2009 to 2010
$975k
Wireless, optical neuromodulation for motion disordersR43NS070453 · NINDS · FERRO SOLUTIONS, INC. · PI OHANDLEY, ROBERT C. · 2010 to 2011
$699k
NIDA NIH HHS 1R01DA029639NIDA NIH HHS R01 DA029639NIDCR NIH HHS 1RC2DE020919NIDCR NIH HHS RC2 DE020919NIH HHS DP2 OD002002NIH HHS DP2OD002002NIMH NIH HHS 1RC1MH088182NIMH NIH HHS RC1 MH088182NINDS NIH HHS 1R01NS067199NINDS NIH HHS 1R43NS070453NINDS NIH HHS R01 NS067199NINDS NIH HHS R43 NS070453
6 · The paper itself

Abstract

The life and operation of cells involve many physiological processes that take place over fast timescales of milliseconds to minutes. Genetically encoded technologies for driving or suppressing specific fast physiological processes in intact cells, perhaps embedded within intact tissues in living organisms, are critical for the ability to understand how these physiological processes contribute to emergent cellular and organismal functions and behaviors. Such "synthetic physiology" tools are often incredibly complex molecular machines, in part because they must operate at high speeds, without causing side effects. We here explore how synthetic physiology molecules can be identified and deployed in cells, and how the physiology of these molecules in cellular contexts can be assessed and optimized. For concreteness, we discuss these methods in the context of the "optogenetic" light-gated ion channels and pumps that we have developed over the past few years as synthetic physiology tools and widely disseminated for use in neuroscience for probing the role of specific brain cell types in neural computations, behaviors, and pathologies. We anticipate that some of the insights revealed here may be of general value for the field of synthetic physiology, as they raise issues that will be of importance for the development and use of high-performance, high-speed, side-effect free physiological control tools in heterologous expression systems.

Indexed as

Cell Physiological PhenomenaAnimalsBiological AssayCell LineHumansIon ChannelsLightOpsinsSynthetic BiologyTime FactorsIon ChannelsOpsins

Identifiers

PMID21601097
PMCPMC3549548
OpenAlexW2370991708

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.