Literature DB >> 34782184

Genetically encoded intrabodies as high-precision tools to visualize and manipulate neuronal function.

James S Trimmer1.   

Abstract

Basic neuroscience research employs numerous forms of antibodies as key reagents in diverse applications. While the predominant use of antibodies is as immunolabeling reagents, neuroscientists are making increased use of intracellular antibodies or intrabodies. Intrabodies are recombinant antibodies genetically encoded for expression within neurons. These can be used to target various cargo (fluorescent proteins, reporters, enzymes, etc.) to specific molecules and subcellular domains to report on and manipulate neuronal function with high precision. Intrabodies have the advantages inherent in all genetically encoded recombinant antibodies but represent a distinct subclass in that their structure allows for their expression and function within cells. The high precision afforded by the ability to direct their expression to specific cell types, and the selective binding of intrabodies to targets within these allows intrabodies to offer unique advantages for neuroscience research, given the tremendous molecular, cellular and morphological complexity of brain neurons. Intrabodies expressed within neurons have been used for a variety of purposes in basic neuroscience research. Here I provide a general background to intrabodies and their development, and examples of their emerging utility as valuable basic neuroscience research tools.
Copyright © 2021. Published by Elsevier Ltd.

Entities:  

Keywords:  Brain; FingR; Intrabody; Live cell imaging; Nanobody; Neuron; Plasmid; Recombinant; ScFv

Mesh:

Substances:

Year:  2021        PMID: 34782184      PMCID: PMC9086100          DOI: 10.1016/j.semcdb.2021.11.004

Source DB:  PubMed          Journal:  Semin Cell Dev Biol        ISSN: 1084-9521            Impact factor:   7.499


  79 in total

1.  Identification of the Kv2.1 K+ channel as a major component of the delayed rectifier K+ current in rat hippocampal neurons.

Authors:  H Murakoshi; J S Trimmer
Journal:  J Neurosci       Date:  1999-03-01       Impact factor: 6.167

2.  Structural and thermodynamic analysis of the GFP:GFP-nanobody complex.

Authors:  Marta H Kubala; Oleksiy Kovtun; Kirill Alexandrov; Brett M Collins
Journal:  Protein Sci       Date:  2010-12       Impact factor: 6.725

3.  Getting to reproducible antibodies: the rationale for sequenced recombinant characterized reagents.

Authors:  Andrew R M Bradbury; Andreas Plückthun
Journal:  Protein Eng Des Sel       Date:  2015-10       Impact factor: 1.650

4.  Recombinant probes reveal dynamic localization of CaMKIIα within somata of cortical neurons.

Authors:  Rudy J Mora; Richard W Roberts; Don B Arnold
Journal:  J Neurosci       Date:  2013-09-04       Impact factor: 6.167

5.  Recombinant Antibodies in Basic Neuroscience Research.

Authors:  James S Trimmer
Journal:  Curr Protoc Neurosci       Date:  2020-12

6.  Gene Expression Profiling with Cre-Conditional Pseudorabies Virus Reveals a Subset of Midbrain Neurons That Participate in Reward Circuitry.

Authors:  Lisa E Pomeranz; Mats I Ekstrand; Kaamashri N Latcha; Gregory A Smith; Lynn W Enquist; Jeffrey M Friedman
Journal:  J Neurosci       Date:  2017-03-10       Impact factor: 6.167

7.  Efficient gene transfer into the embryonic mouse brain using in vivo electroporation.

Authors:  T Saito; N Nakatsuji
Journal:  Dev Biol       Date:  2001-12-01       Impact factor: 3.582

8.  Distinct Ca2+ sources in dendritic spines of hippocampal CA1 neurons couple to SK and Kv4 channels.

Authors:  Kang Wang; Mike T Lin; John P Adelman; James Maylie
Journal:  Neuron       Date:  2014-01-22       Impact factor: 17.173

9.  Distance-dependent gradient in NMDAR-driven spine calcium signals along tapering dendrites.

Authors:  Alison S Walker; Guilherme Neves; Federico Grillo; Rachel E Jackson; Mark Rigby; Cian O'Donnell; Andrew S Lowe; Gema Vizcay-Barrena; Roland A Fleck; Juan Burrone
Journal:  Proc Natl Acad Sci U S A       Date:  2017-02-16       Impact factor: 11.205

10.  Relocation of an Extrasynaptic GABAA Receptor to Inhibitory Synapses Freezes Excitatory Synaptic Strength and Preserves Memory.

Authors:  Christopher M Davenport; Rajit Rajappa; Ljudmila Katchan; Charlotte R Taylor; Ming-Chi Tsai; Caleb M Smith; Johannes W de Jong; Don B Arnold; Stephan Lammel; Richard H Kramer
Journal:  Neuron       Date:  2020-10-22       Impact factor: 17.173

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