Literature DB >> 33604571

Development of novel bioassays to detect soluble and aggregated Huntingtin proteins on three technology platforms.

Christian Landles1, Rebecca E Milton1, Alexandre Jean2, Stuart McLarnon2, Sean J McAteer1, Bridget A Taxy1, Georgina F Osborne1, Chuangchuang Zhang3,4, Wenzhen Duan3,4, David Howland5, Gillian P Bates1.   

Abstract

Huntington's disease is caused by a CAG / polyglutamine repeat expansion. Mutated CAG repeats undergo somatic instability, resulting in tracts of several hundred CAGs in the brain; and genetic modifiers of Huntington's disease have indicated that somatic instability is a major driver of age of onset and disease progression. As the CAG repeat expands, the likelihood that exon 1 does not splice to exon 2 increases, resulting in two transcripts that encode full-length huntingtin protein, as well as the highly pathogenic and aggregation-prone exon 1 huntingtin protein. Strategies that target the huntingtin gene or transcripts are a major focus of therapeutic development. It is essential that the levels of all isoforms of huntingtin protein can be tracked, to better understand the molecular pathogenesis, and to assess the impact of huntingtin protein-lowering approaches in preclinical studies and clinical trials. Huntingtin protein bioassays for soluble and aggregated forms of huntingtin protein are in widespread use on the homogeneous time-resolved fluorescence and Meso Scale Discovery platforms, but these do not distinguish between exon 1 huntingtin protein and full-length huntingtin protein. In addition, they are frequently used to quantify huntingtin protein levels in the context of highly expanded polyglutamine tracts, for which appropriate protein standards do not currently exist. Here, we set out to develop novel huntingtin protein bioassays to ensure that all soluble huntingtin protein isoforms could be distinguished. We utilized the zQ175 Huntington's disease mouse model that has ∼190 CAGs, a CAG repeat size for which protein standards are not available. Initially, 30 combinations of six antibodies were tested on three technology platforms: homogeneous time-resolved fluorescence, amplified luminescent proximity homogeneous assay and Meso Scale Discovery, and a triage strategy was employed to select the best assays. We found that, without a polyglutamine-length-matched standard, the vast majority of soluble mutant huntingtin protein assays cannot be used for quantitative purposes, as the highly expanded polyglutamine tract decreased assay performance. The combination of our novel assays, with those already in existence, provides a tool-kit to track: total soluble mutant huntingtin protein, soluble exon 1 huntingtin protein, soluble mutant huntingtin protein (excluding the exon 1 huntingtin protein) and total soluble full-length huntingtin protein (mutant and wild type). Several novel aggregation assays were also developed that track with disease progression. These selected assays can be used to compare the levels of huntingtin protein isoforms in a wide variety of mouse models of Huntington's disease and to determine how these change in response to genetic or therapeutic manipulations.
© The Author(s) (2021). Published by Oxford University Press on behalf of the Guarantors of Brain.

Entities:  

Keywords:  Huntington’s disease; huntingtin aggregation; huntingtin bioassay; polyglutamine; zQ175 knock-in mouse model

Year:  2021        PMID: 33604571      PMCID: PMC7878250          DOI: 10.1093/braincomms/fcaa231

Source DB:  PubMed          Journal:  Brain Commun        ISSN: 2632-1297


  39 in total

1.  Aggregation of huntingtin in neuronal intranuclear inclusions and dystrophic neurites in brain.

Authors:  M DiFiglia; E Sapp; K O Chase; S W Davies; G P Bates; J P Vonsattel; N Aronin
Journal:  Science       Date:  1997-09-26       Impact factor: 47.728

2.  Widespread heterogeneous neuronal loss across the cerebral cortex in Huntington's disease.

Authors:  Alissa L Nana; Eric H Kim; Doris C V Thu; Dorothy E Oorschot; Lynette J Tippett; Virginia M Hogg; Beth J Synek; Richard Roxburgh; Henry J Waldvogel; Richard L M Faull
Journal:  J Huntingtons Dis       Date:  2014

3.  Huntingtin-encoded polyglutamine expansions form amyloid-like protein aggregates in vitro and in vivo.

Authors:  E Scherzinger; R Lurz; M Turmaine; L Mangiarini; B Hollenbach; R Hasenbank; G P Bates; S W Davies; H Lehrach; E E Wanker
Journal:  Cell       Date:  1997-08-08       Impact factor: 41.582

4.  Aberrant splicing of HTT generates the pathogenic exon 1 protein in Huntington disease.

Authors:  Kirupa Sathasivam; Andreas Neueder; Theresa A Gipson; Christian Landles; Agnesska C Benjamin; Marie K Bondulich; Donna L Smith; Richard L M Faull; Raymund A C Roos; David Howland; Peter J Detloff; David E Housman; Gillian P Bates
Journal:  Proc Natl Acad Sci U S A       Date:  2013-01-22       Impact factor: 11.205

Review 5.  Huntington disease.

Authors:  Gillian P Bates; Ray Dorsey; James F Gusella; Michael R Hayden; Chris Kay; Blair R Leavitt; Martha Nance; Christopher A Ross; Rachael I Scahill; Ronald Wetzel; Edward J Wild; Sarah J Tabrizi
Journal:  Nat Rev Dis Primers       Date:  2015-04-23       Impact factor: 52.329

6.  Intranuclear inclusions and neuritic aggregates in transgenic mice expressing a mutant N-terminal fragment of huntingtin.

Authors:  G Schilling; M W Becher; A H Sharp; H A Jinnah; K Duan; J A Kotzuk; H H Slunt; T Ratovitski; J K Cooper; N A Jenkins; N G Copeland; D L Price; C A Ross; D R Borchelt
Journal:  Hum Mol Genet       Date:  1999-03       Impact factor: 6.150

Review 7.  Huntingtin Lowering Strategies for Disease Modification in Huntington's Disease.

Authors:  Sarah J Tabrizi; Rhia Ghosh; Blair R Leavitt
Journal:  Neuron       Date:  2019-03-06       Impact factor: 17.173

8.  Spatiotemporal Proteomic Profiling of Huntington's Disease Inclusions Reveals Widespread Loss of Protein Function.

Authors:  Fabian Hosp; Sara Gutiérrez-Ángel; Martin H Schaefer; Jürgen Cox; Felix Meissner; Mark S Hipp; F-Ulrich Hartl; Rüdiger Klein; Irina Dudanova; Matthias Mann
Journal:  Cell Rep       Date:  2017-11-21       Impact factor: 9.423

9.  CAG Repeat Not Polyglutamine Length Determines Timing of Huntington's Disease Onset.

Authors: 
Journal:  Cell       Date:  2019-08-08       Impact factor: 41.582

10.  Quantification assays for total and polyglutamine-expanded huntingtin proteins.

Authors:  Douglas Macdonald; Michela A Tessari; Ivette Boogaard; Melanie Smith; Kristiina Pulli; Agnieszka Szynol; Faywell Albertus; Marieke B A C Lamers; Sipke Dijkstra; Daniel Kordt; Wolfgang Reindl; Frank Herrmann; George McAllister; David F Fischer; Ignacio Munoz-Sanjuan
Journal:  PLoS One       Date:  2014-05-09       Impact factor: 3.240

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  2 in total

1.  Development of mAb-based polyglutamine-dependent and polyglutamine length-independent huntingtin quantification assays with cross-site validation.

Authors:  David F Fischer; Sipke Dijkstra; Kimberly Lo; Johnny Suijker; Ana C P Correia; Patricia Naud; Martin Poirier; Michela A Tessari; Ivette Boogaard; Geraldine Flynn; Mijke Visser; Marieke B A C Lamers; George McAllister; Ignacio Munoz-Sanjuan; Douglas Macdonald
Journal:  PLoS One       Date:  2022-04-08       Impact factor: 3.240

2.  Use of high-content imaging to quantify transduction of AAV-PHP viruses in the brain following systemic delivery.

Authors:  Edward J Smith; Pamela P Farshim; Rachel Flomen; Samuel T Jones; Sean J McAteer; Benjamin E Deverman; Viviana Gradinaru; Gillian P Bates
Journal:  Brain Commun       Date:  2021-05-17
  2 in total

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