期刊
ACS CHEMICAL BIOLOGY
卷 9, 期 5, 页码 1197-1203出版社
AMER CHEMICAL SOC
DOI: 10.1021/cb400849n
关键词
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资金
- MEXT [3306, 23115003]
- JST
- Takeda Science Foundation
- JSPS [21687007]
- Grants-in-Aid for Scientific Research [21687007] Funding Source: KAKEN
Calcium ion (Ca2+) is an important second messenger implicated in the control of many different cellular processes in living organisms. Ca2+ is typically studied by direct visualization using chemically or genetically encoded indicators. A complementary, and perhaps more useful, approach involves direct manipulation of Ca2+ concentration; tools for this exist but are rather poorly developed compared to the indicators at least. Here, we report a photoactivatable Ca2+-releasing protein, photoactivatable Ca2+ releaser (PACR), made by the insertion of a photosensitive protein domain (LOV2) into a Ca2+ binding protein (calmodulin fused with the M13 peptide). As the PACR is genetically encoded, and unlike conventional optical control tools (e.g., channel rhodopsin) not membrane bound, we are able to restrict expression within the cell, to allow subcellular perturbation of Ca2+ levels. In whole animals, we are able to control the behavior of Caenorhabditis elegans with light by expressing the PACR only in the touch neuron.
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