Literature DB >> 30735172

A Rhodopsin Transport Assay by High-Content Imaging Analysis.

Bing Feng1, Xujie Liu1, Yuanyuan Chen2.   

Abstract

Rhodopsin misfolding mutations lead to rod photoreceptor death that is manifested as autosomal dominant retinitis pigmentosa (RP), a progressive blinding disease that lacks effective treatment. We hypothesize that the cytotoxicity of the misfolded rhodopsin mutant can be alleviated by pharmacologically stabilizing the mutant rhodopsin protein. The P23H mutation, among the other Class II rhodopsin mutations, encodes a structurally unstable rhodopsin mutant protein that is accumulated in the endoplasmic reticulum (ER), whereas the wild type rhodopsin is transported to the plasma membrane in mammalian cells. We previously performed a luminescence-based high-throughput screen (HTS) and identified a group of pharmacological chaperones that rescued the transport of the P23H rhodopsin from ER to the plasma membrane. Here, using an immunostaining method followed by a high-content imaging analysis, we quantified the mutant rhodopsin protein amount in the whole cell and on the plasma membrane. This method is informative and effective to identify true hits from false positives following HTS. Additionally, the high-content image analysis enabled us to quantify multiple parameters from a single experiment to evaluate the pharmacological properties of each compound. Using this assay, we analyzed the effect of 11 different compounds towards six RP associated rhodopsin mutants, obtaining a 2-D pharmacological profile for a quantitative and qualitative understanding about the structural stability of these rhodopsin mutants and efficacy of different compounds towards these mutants.

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Year:  2019        PMID: 30735172      PMCID: PMC6518421          DOI: 10.3791/58703

Source DB:  PubMed          Journal:  J Vis Exp        ISSN: 1940-087X            Impact factor:   1.355


  22 in total

1.  A Simple Statistical Parameter for Use in Evaluation and Validation of High Throughput Screening Assays.

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Journal:  J Biomol Screen       Date:  1999

2.  Anti-rhodopsin monoclonal antibodies of defined specificity: characterization and application.

Authors:  G Adamus; Z S Zam; A Arendt; K Palczewski; J H McDowell; P A Hargrave
Journal:  Vision Res       Date:  1991       Impact factor: 1.886

3.  Functional heterogeneity of mutant rhodopsins responsible for autosomal dominant retinitis pigmentosa.

Authors:  C H Sung; B G Schneider; N Agarwal; D S Papermaster; J Nathans
Journal:  Proc Natl Acad Sci U S A       Date:  1991-10-01       Impact factor: 11.205

4.  Molecular mechanisms of rhodopsin retinitis pigmentosa and the efficacy of pharmacological rescue.

Authors:  Mark P Krebs; David C Holden; Parth Joshi; Charles L Clark; Andrew H Lee; Shalesh Kaushal
Journal:  J Mol Biol       Date:  2009-11-11       Impact factor: 5.469

Review 5.  The molecular and cellular basis of rhodopsin retinitis pigmentosa reveals potential strategies for therapy.

Authors:  Dimitra Athanasiou; Monica Aguila; James Bellingham; Wenwen Li; Caroline McCulley; Philip J Reeves; Michael E Cheetham
Journal:  Prog Retin Eye Res       Date:  2017-10-16       Impact factor: 21.198

6.  High-throughput screening assays to identify small molecules preventing photoreceptor degeneration caused by the rhodopsin P23H mutation.

Authors:  Yuanyuan Chen; Hong Tang
Journal:  Methods Mol Biol       Date:  2015

7.  Rhodopsin mutations responsible for autosomal dominant retinitis pigmentosa. Clustering of functional classes along the polypeptide chain.

Authors:  C H Sung; C M Davenport; J Nathans
Journal:  J Biol Chem       Date:  1993-12-15       Impact factor: 5.157

8.  Pharmacological chaperone-mediated in vivo folding and stabilization of the P23H-opsin mutant associated with autosomal dominant retinitis pigmentosa.

Authors:  Syed M Noorwez; Vladimir Kuksa; Yoshikazu Imanishi; Li Zhu; Sławomir Filipek; Krzysztof Palczewski; Shalesh Kaushal
Journal:  J Biol Chem       Date:  2003-02-01       Impact factor: 5.157

Review 9.  The Human Gene Mutation Database: towards a comprehensive repository of inherited mutation data for medical research, genetic diagnosis and next-generation sequencing studies.

Authors:  Peter D Stenson; Matthew Mort; Edward V Ball; Katy Evans; Matthew Hayden; Sally Heywood; Michelle Hussain; Andrew D Phillips; David N Cooper
Journal:  Hum Genet       Date:  2017-03-27       Impact factor: 4.132

10.  A novel small molecule chaperone of rod opsin and its potential therapy for retinal degeneration.

Authors:  Yuanyuan Chen; Yu Chen; Beata Jastrzebska; Marcin Golczak; Sahil Gulati; Hong Tang; William Seibel; Xiaoyu Li; Hui Jin; Yong Han; Songqi Gao; Jianye Zhang; Xujie Liu; Hossein Heidari-Torkabadi; Phoebe L Stewart; William E Harte; Gregory P Tochtrop; Krzysztof Palczewski
Journal:  Nat Commun       Date:  2018-05-17       Impact factor: 14.919

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  1 in total

1.  Nonretinoid chaperones improve rhodopsin homeostasis in a mouse model of retinitis pigmentosa.

Authors:  Abhishek Vats; Yibo Xi; Bing Feng; Owen D Clinger; Anthony J St Leger; Xujie Liu; Archisha Ghosh; Chase D Dermond; Kira L Lathrop; Gregory P Tochtrop; Serge Picaud; Yuanyuan Chen
Journal:  JCI Insight       Date:  2022-05-23
  1 in total

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