Linda Boland - US grants
Affiliations: | Univ Richmond |
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The funding information displayed below comes from the NIH Research Portfolio Online Reporting Tools and the NSF Award Database.The grant data on this page is limited to grants awarded in the United States and is thus partial. It can nonetheless be used to understand how funding patterns influence mentorship networks and vice-versa, which has deep implications on how research is done.
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High-probability grants
According to our matching algorithm, Linda Boland is the likely recipient of the following grants.Years | Recipients | Code | Title / Keywords | Matching score |
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2001 — 2004 | O'grady, Scott (co-PI) [⬀] Feddersen, Rod Kofuji, Paulo (co-PI) [⬀] Boland, Linda |
N/AActivity Code Description: No activity code was retrieved: click on the grant title for more information |
Acquisition of Instrumentation For Ion Channel Research and Research Training @ University of Minnesota-Twin Cities ABSTRACT |
0.907 |
2011 — 2015 | Boland, Linda M | R15Activity Code Description: Supports small-scale research projects at educational institutions that provide baccalaureate or advanced degrees for a significant number of the Nation’s research scientists but that have not been major recipients of NIH support. The goals of the program are to (1) support meritorious research, (2) expose students to research, and (3) strengthen the research environment of the institution. Awards provide limited Direct Costs, plus applicable F&A costs, for periods not to exceed 36 months. This activity code uses multi-year funding authority; however, OER approval is NOT needed prior to an IC using this activity code. |
Lipid Modulation of Potassium Channels @ University of Richmond DESCRIPTION (provided by applicant): Our project focuses on how potassium ion channels are modified by the actions of lipids including polyphosphoinositides and polyunsaturated fatty acids. These two classes of lipids are structural components of the cellular membrane and also act as lipid signals following certain forms of cellular communication. The fatty acids are present in oily fish, and their consumption is promoted as part of a healthy heart diet. This research has important health implications for how lipid signals impact the proper rhythmicity of heart muscle, neuronal firing patterns, memory disorders, pain and anesthesia, epilepsy, and ischemic damage during stroke and heart attack. To better understand the molecular basis for how these lipids regulate the electrical activity of cells, we will study two channels known as Kir and K2P. We use channels cloned from sponges, a valuable animal model organism, because they give us a way to understand human ion channels by comparative analysis. We will determine how the Kir channel from sponge is regulated by different polyphosphoinositides and compare this to the effects of these lipids on vertebrate ion channels. We found that the Kir channels can be modified by activating enzymes that add phosphate groups to proteins; we will determine how this phosphorylation event may interact with the regulation of the channel by lipid signals. We made a computer model of the sponge Kir channel, at the atomic level, based on atomic structural data for vertebrate Kir channels. We use this model to help predict how the lipids interact with the channel, how phosphorylation may interact with the lipids, and what specific parts of the channel may be important in determining the type of lipid that can interact with the channel. We also plan to measure the lipids in sponge cells and to investigate information in the sponge genome to predict which of the different types of these lipids may exist in the native environment of the channels. For a second type of channel known as K2P, we found that opening of the sponge channel requires the fatty acid, arachidonic acid. Previous work on fatty acid effects in vertebrate channels has implicated a certain region of the K2P channel. We will examine the role of this region for the sponge K2P channel activation by fatty acids using molecular approaches and electrophysiology. Overall, this project will help us better understand the structure-function relationships of lipid signals and ion channels. The principal investigator s an experienced ion channel biologist who has successfully mentored 40 undergraduate research students in almost 10 years at the University of Richmond. In addition to the research goals, this project provides undergraduates with meaningful research experiences and they contribute to biomedically important research, which is the main goal of the AREA grant program. |
0.922 |