Literature DB >> 23317763

CFTR-mutation specific applications of CFTR-directed monoclonal antibodies.

M A van Meegen1, S W J Terheggen, K J Koymans, L A W Vijftigschild, J F Dekkers, C K van der Ent, J M Beekman.   

Abstract

BACKGROUND: Over the last decade novel monoclonal CFTR-specific antibodies have been developed. We here present a paired analysis to detect wild-type and mutant CFTR using Western blot analysis, flow cytometry and confocal microscopy in several cellular expression systems.
METHODS: The following CFTR-specific antibodies were used; 217, 432, 450, 570, 769, 596, 660, L12B4 and 24.1. Mutant CFTR was detected in HEK293 cells transiently expressing the mutations; G542X, R1162X, F508del, N1303K, G551D, R117H, A455E.
RESULTS: The majority of these antibodies are suitable for most applications tested. Using immunofluorescence, some antibodies can better detect mutant forms of CFTR (F508del and N1303K by mAbs 596 and 769), or display lower aspecific detection by Western blot analysis (mAbs 432, 450, 769 and 596) or immunofluorescence (mAbs 432, 450, 570 and 769).
CONCLUSION: Optimal detection of CFTR by monoclonal antibodies depends on CFTR mutation and the specific research application.
Copyright © 2012 European Cystic Fibrosis Society. Published by Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Confocal microscopy; Flow cytometry; Monoclonal antibodies; Mutant CFTR; Paired analysis; Western blot

Mesh:

Substances:

Year:  2013        PMID: 23317763     DOI: 10.1016/j.jcf.2012.12.005

Source DB:  PubMed          Journal:  J Cyst Fibros        ISSN: 1569-1993            Impact factor:   5.482


  11 in total

1.  In Situ Analysis Reveals That CFTR Is Expressed in Only a Small Minority of β-Cells in Normal Adult Human Pancreas.

Authors:  Michael G White; Rashmi R Maheshwari; Scott J Anderson; Rolando Berlinguer-Palmini; Claire Jones; Sarah J Richardson; Pavana G Rotti; Sarah L Armour; Yuchun Ding; Natalio Krasnogor; John F Engelhardt; Mike A Gray; Noel G Morgan; James A M Shaw
Journal:  J Clin Endocrinol Metab       Date:  2020-05-01       Impact factor: 5.958

2.  Precise Targeting of miRNA Sites Restores CFTR Activity in CF Bronchial Epithelial Cells.

Authors:  Chiara De Santi; Elena Fernández Fernández; Rachel Gaul; Sebastian Vencken; Arlene Glasgow; Irene K Oglesby; Killian Hurley; Finn Hawkins; Nilay Mitash; Fangping Mu; Rana Raoof; David C Henshall; Meritxell B Cutrona; Jeremy C Simpson; Brian J Harvey; Barry Linnane; Paul McNally; Sally Ann Cryan; Ronan MacLoughlin; Agnieszka Swiatecka-Urban; Catherine M Greene
Journal:  Mol Ther       Date:  2020-02-06       Impact factor: 11.454

3.  Cystic fibrosis-related diabetes is caused by islet loss and inflammation.

Authors:  Nathaniel J Hart; Radhika Aramandla; Gregory Poffenberger; Cody Fayolle; Ariel H Thames; Austin Bautista; Aliya F Spigelman; Jenny Aurielle B Babon; Megan E DeNicola; Prasanna K Dadi; William S Bush; Appakalai N Balamurugan; Marcela Brissova; Chunhua Dai; Nripesh Prasad; Rita Bottino; David A Jacobson; Mitchell L Drumm; Sally C Kent; Patrick E MacDonald; Alvin C Powers
Journal:  JCI Insight       Date:  2018-04-19

Review 4.  Survival in a bad neighborhood: pancreatic islets in cystic fibrosis.

Authors:  Andrew W Norris; Katie Larson Ode; Lina Merjaneh; Srinath Sanda; Yaling Yi; Xingshen Sun; John F Engelhardt; Rebecca L Hull
Journal:  J Endocrinol       Date:  2019-02-01       Impact factor: 4.286

5.  Cyclodextrins reduce the ability of Pseudomonas aeruginosa outer-membrane vesicles to reduce CFTR Cl- secretion.

Authors:  Roxanna Barnaby; Katja Koeppen; Bruce A Stanton
Journal:  Am J Physiol Lung Cell Mol Physiol       Date:  2018-10-25       Impact factor: 5.464

6.  The CFTR P67L variant reveals a key role for N-terminal lasso helices in channel folding, maturation, and pharmacologic rescue.

Authors:  Carleen Mae Sabusap; Disha Joshi; Luba Simhaev; Kathryn E Oliver; Hanoch Senderowitz; Marcel van Willigen; Ineke Braakman; Andras Rab; Eric J Sorscher; Jeong S Hong
Journal:  J Biol Chem       Date:  2021-03-26       Impact factor: 5.486

7.  Human extrahepatic and intrahepatic cholangiocyte organoids show region-specific differentiation potential and model cystic fibrosis-related bile duct disease.

Authors:  Monique M A Verstegen; Floris J M Roos; Ksenia Burka; Helmuth Gehart; Myrthe Jager; Maaike de Wolf; Marcel J C Bijvelds; Hugo R de Jonge; Arif I Ardisasmita; Nick A van Huizen; Henk P Roest; Jeroen de Jonge; Michael Koch; Francesco Pampaloni; Sabine A Fuchs; Imre F Schene; Theo M Luider; Hubert P J van der Doef; Frank A J A Bodewes; Ruben H J de Kleine; Bart Spee; Gert-Jan Kremers; Hans Clevers; Jan N M IJzermans; Edwin Cuppen; Luc J W van der Laan
Journal:  Sci Rep       Date:  2020-12-14       Impact factor: 4.379

8.  Positional effects of premature termination codons on the biochemical and biophysical properties of CFTR.

Authors:  Jiunn-Tyng Yeh; Tzyh-Chang Hwang
Journal:  J Physiol       Date:  2019-11-02       Impact factor: 5.182

9.  Apical CFTR expression in human nasal epithelium correlates with lung disease in cystic fibrosis.

Authors:  Marit Arianne van Meegen; Suzanne Willemina Julia Terheggen-Lagro; Kirsten Judith Koymans; Cornelis Korstiaan van der Ent; Jeffrey Matthijn Beekman
Journal:  PLoS One       Date:  2013-03-06       Impact factor: 3.240

10.  A Peptide Nucleic Acid (PNA) Masking the miR-145-5p Binding Site of the 3'UTR of the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) mRNA Enhances CFTR Expression in Calu-3 Cells.

Authors:  Shaiq Sultan; Andrea Rozzi; Jessica Gasparello; Alex Manicardi; Roberto Corradini; Chiara Papi; Alessia Finotti; Ilaria Lampronti; Eva Reali; Giulio Cabrini; Roberto Gambari; Monica Borgatti
Journal:  Molecules       Date:  2020-04-05       Impact factor: 4.411

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