دورية أكاديمية

High throughput analysis of vacuolar acidification.

التفاصيل البيبلوغرافية
العنوان: High throughput analysis of vacuolar acidification.
المؤلفون: Zhang C; Department of Biochemistry, University of Illinois Urbana-Champaign, Urbana, IL, 61801, USA., Balutowski A; Department of Biochemistry, University of Illinois Urbana-Champaign, Urbana, IL, 61801, USA., Feng Y; Department of Biochemistry, University of Illinois Urbana-Champaign, Urbana, IL, 61801, USA., Calderin JD; Department of Biochemistry, University of Illinois Urbana-Champaign, Urbana, IL, 61801, USA., Fratti RA; Department of Biochemistry, University of Illinois Urbana-Champaign, Urbana, IL, 61801, USA; Center for Biophysics and Quantitative Biology, University of Illinois Urbana-Champaign, Urbana, IL, 61801, USA. Electronic address: rfratti@illinois.edu.
المصدر: Analytical biochemistry [Anal Biochem] 2022 Dec 01; Vol. 658, pp. 114927. Date of Electronic Publication: 2022 Sep 24.
نوع المنشور: Journal Article; Research Support, U.S. Gov't, Non-P.H.S.; Research Support, N.I.H., Extramural
اللغة: English
بيانات الدورية: Publisher: Elsevier Country of Publication: United States NLM ID: 0370535 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1096-0309 (Electronic) Linking ISSN: 00032697 NLM ISO Abbreviation: Anal Biochem Subsets: MEDLINE
أسماء مطبوعة: Publication: <2000- > : San Diego, CA : Elsevier
Original Publication: Orlando Fl : Academic Press
مواضيع طبية MeSH: Acridine Orange* , Vacuolar Proton-Translocating ATPases*, Vacuoles ; Endosomes/metabolism ; Saccharomyces cerevisiae/metabolism ; Lysosomes/metabolism ; Hydrogen-Ion Concentration
مستخلص: Eukaryotic cells are compartmentalized into membrane-bound organelles, allowing each organelle to maintain the specialized conditions needed for their specific functions. One of the features that change between organelles is lumenal pH. In the endocytic and secretory pathways, lumenal pH is controlled by isoforms and concentration of the vacuolar-type H + -ATPase (V-ATPase). In the endolysosomal pathway, copies of complete V-ATPase complexes accumulate as membranes mature from early endosomes to late endosomes and lysosomes. Thus, each compartment becomes more acidic as maturation proceeds. Lysosome acidification is essential for the breakdown of macromolecules delivered from endosomes as well as cargo from different autophagic pathways, and dysregulation of this process is linked to various diseases. Thus, it is important to understand the regulation of the V-ATPase. Here we describe a high-throughput method for screening inhibitors/activators of V-ATPase activity using Acridine Orange (AO) as a fluorescent reporter for acidified yeast vacuolar lysosomes. Through this method, the acidification of purified vacuoles can be measured in real-time in half-volume 96-well plates or a larger 384-well format. This not only reduces the cost of expensive low abundance reagents, but it drastically reduces the time needed to measure individual conditions in large volume cuvettes.
(Copyright © 2022 Elsevier Inc. All rights reserved.)
التعليقات: Erratum in: Anal Biochem. 2022 Nov 18;661:114984. (PMID: 36410101)
معلومات مُعتمدة: T32 GM070421 United States GM NIGMS NIH HHS
فهرسة مساهمة: Keywords: Acridine orange; Gadolinium; Lanthanum; Lysosome; Nickel; V-ATPase; Vph1
المشرفين على المادة: F30N4O6XVV (Acridine Orange)
EC 3.6.1.- (Vacuolar Proton-Translocating ATPases)
تواريخ الأحداث: Date Created: 20220927 Date Completed: 20221025 Latest Revision: 20221130
رمز التحديث: 20231215
DOI: 10.1016/j.ab.2022.114927
PMID: 36167157
قاعدة البيانات: MEDLINE
الوصف
تدمد:1096-0309
DOI:10.1016/j.ab.2022.114927