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Using Fluorescent GAP Indicators to Monitor ER Ca 2 .
- Source :
-
Current protocols [Curr Protoc] 2024 Jun; Vol. 4 (6), pp. e1060. - Publication Year :
- 2024
-
Abstract
- The endoplasmic reticulum (ER) is the main reservoir of Ca <superscript>2+</superscript> of the cell. Accurate and quantitative measuring of Ca <superscript>2+</superscript> dynamics within the lumen of the ER has been challenging. In the last decade a few genetically encoded Ca <superscript>2+</superscript> indicators have been developed, including a family of fluorescent Ca <superscript>2+</superscript> indicators, dubbed GFP-Aequorin Proteins (GAPs). They are based on the fusion of two jellyfish proteins, the green fluorescent protein (GFP) and the Ca <superscript>2+</superscript> -binding protein aequorin. GAP Ca <superscript>2+</superscript> indicators exhibit a combination of several features: they are excitation ratiometric indicators, with reciprocal changes in the fluorescence excited at 405 and 470 nm, which is advantageous for imaging experiments; they exhibit a Hill coefficient of 1, which facilitates the calibration of the fluorescent signal into Ca <superscript>2+</superscript> concentrations; they are insensible to variations in the Mg <superscript>2+</superscript> concentrations or pH variations (in the 6.5-8.5 range); and, due to the lack of mammalian homologues, these proteins have a favorable expression in transgenic animals. A low Ca <superscript>2+</superscript> affinity version of GAP, GAP3 (K <subscript>D</subscript> ≅ 489 µM), has been engineered to conform with the estimated [Ca <superscript>2+</superscript> ] in the ER. GAP3 targeted to the lumen of the ER (erGAP3) can be utilized for imaging intraluminal Ca <superscript>2+</superscript> . The ratiometric measurements provide a quantitative method to assess accurate [Ca <superscript>2+</superscript> ] <subscript>ER</subscript> , both dynamically and at rest. In addition, erGAP3 can be combined with synthetic cytosolic Ca <superscript>2+</superscript> indicators to simultaneously monitor ER and cytosolic Ca <superscript>2+</superscript> . Here, we provide detailed methods to assess erGAP3 expression and to perform Ca <superscript>2+</superscript> imaging, either restricted to the ER lumen, or simultaneously in the ER and the cytosol. © 2024 The Authors. Current Protocols published by Wiley Periodicals LLC. Basic Protocol 1: Detection of erGAP3 in the ER by immunofluorescence Basic Protocol 2: Monitoring ER Ca <superscript>2+</superscript> Basic Protocol 3: Monitoring ER- and cytosolic-Ca <superscript>2+</superscript> Support Protocol: Generation of a stable cell line expressing erGAP3.<br /> (© 2024 The Authors. Current Protocols published by Wiley Periodicals LLC.)
Details
- Language :
- English
- ISSN :
- 2691-1299
- Volume :
- 4
- Issue :
- 6
- Database :
- MEDLINE
- Journal :
- Current protocols
- Publication Type :
- Academic Journal
- Accession number :
- 38923371
- Full Text :
- https://doi.org/10.1002/cpz1.1060