Olfactory receptor-based sensors for biomedical applications
用于生物医学应用的基于嗅觉受体的传感器
基本信息
- 批准号:9382072
- 负责人:
- 金额:$ 36.35万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2017
- 资助国家:美国
- 起止时间:2017-09-01 至 2022-08-31
- 项目状态:已结题
- 来源:
- 关键词:AwardBindingBiologicalBiological MarkersBiological ProcessBiotechnologyCell Surface ReceptorsCell surfaceChemicalsChemotaxisColonDetectionDevelopmentDiagnosisDiseaseEngineeringEnvironmentFamilyFingerprintFutureG-Protein-Coupled ReceptorsGenomeGoalsHealthHumanInjuryInterphaseKidneyLeadLigand BindingLinkLungMedicalMicrobeMicrofluidicsMolecular TargetMuscleMuscle CellsMuscle FibersMyofibrilsNeuromuscular DiseasesOdorsPharmacologic SubstanceProcessProductionReadingReceptor ActivationResearchRoleSamplingTechnologyTherapeuticTissuesYeastsangiogenesisaqueousbasegut microbiotahealinghigh throughput screeningimprovedmicrobialmicrobiomeolfactory receptorpollutantprotein expressionreceptorrepairedscreeningsensortherapeutic target
项目摘要
7. Project Summary/Abstract
Olfactory receptors are one of the largest family of chemical cell-surface receptors in humans, and
ectopically expressed olfactory receptors (exORs) have been found in 16 different tissues, including the lungs,
kidneys and colon. In non-olfactory tissue, exORs do not detect “odors”, but drive a number of biological
process, including chemotaxis, development, and angiogenesis. Understanding the role of exORs in human
health—including which exORs are medically relevant, and what compounds activate exORs in the
endogenous tissues—is a challenging, slow and laborious process. The downstream targets of exORs are
often not known and reading out exORs activation is often not possible. Recently, the Peralta-Yahya group has
developed OR-based sensors in yeast to detect chemicals in the environment for biotechnology applications,
such as the detection of chemical pollutants and biofuels in aqueous medium. By expressing human ORs on
the yeast cell surface and linking OR ligand binding to fluorescent protein expression, this sensor technology
provides a rapid readout for OR activation. In this MIRA proposal, we set forth how the OR-based sensor
technology can expedite and streamline the study of the role of exORs in human health. We will focus on
applying the OR-based sensor technology to the study of exORs present in skeletal muscle cells and in the
colon. In skeletal muscle cells, we will identify the endogenous chemical present in muscle cells that activates
the exOR mOR23 and results in decreased myofibril branching upon muscle repair, resulting in a stronger
repaired muscle. Once identified, the chemical can serve as a lead compound for the synthesis of therapeutics
that improve muscle healing. Further, such a therapeutic may also have implication in the treatment of
neuromuscular diseases where a large number of branched myofibrils are seen. In the colon, we hypothesize
that the gut microbiota communicates with the human host via exORs and that healthy and diseased colons
may different OR activation fingerprints that can be used as biomarkers to diagnose biological conditions.
Identification of the specific ORs activated will provide molecular targets to, in the future, elucidate their
downstream effectors to further understand the role of ORs in gut disease. Additionally, identified ORs could
also function as therapeutic targets; roughly 40% of pharmaceutical targets bind G-protein coupled receptors
(GPCRs), of which ORs are a subset. More generally, knowing which gut metabolites interact with human
receptors, such as ORs, will fill a crucial gap in understanding the microbiome-host interactions. As part of the
MIRA award, we will also interphase the OR-based sensor technology with microfluidics to enable the high-
throughput screening (>107 samples/day) of non-colorimetric/non-fluorescent chemicals produced by microbes.
This screening throughput will allow the application of genome and evolutionary engineering strategies, which
have been shown to dramatically increase the microbial production of colorimetric chemicals. Specifically, we
will apply the technology to increase the microbial production of advanced pharmaceutical intermediates.
7. 项目总结/文摘
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
数据更新时间:{{ journalArticles.updateTime }}
{{
item.title }}
{{ item.translation_title }}
- DOI:
{{ item.doi }} - 发表时间:
{{ item.publish_year }} - 期刊:
- 影响因子:{{ item.factor }}
- 作者:
{{ item.authors }} - 通讯作者:
{{ item.author }}
数据更新时间:{{ journalArticles.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ monograph.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ sciAawards.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ conferencePapers.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ patent.updateTime }}
Pamela Peralta-Yahya其他文献
Pamela Peralta-Yahya的其他文献
{{
item.title }}
{{ item.translation_title }}
- DOI:
{{ item.doi }} - 发表时间:
{{ item.publish_year }} - 期刊:
- 影响因子:{{ item.factor }}
- 作者:
{{ item.authors }} - 通讯作者:
{{ item.author }}
{{ truncateString('Pamela Peralta-Yahya', 18)}}的其他基金
Olfactory receptor-based sensors for biomedical applications
用于生物医学应用的基于嗅觉受体的传感器
- 批准号:
10240662 - 财政年份:2017
- 资助金额:
$ 36.35万 - 项目类别:
Olfactory receptor-based sensors for biomedical applications
用于生物医学应用的基于嗅觉受体的传感器
- 批准号:
10552435 - 财政年份:2017
- 资助金额:
$ 36.35万 - 项目类别:
相似国自然基金
帽结合蛋白(cap binding protein)调控乙烯信号转导的分子机制
- 批准号:32170319
- 批准年份:2021
- 资助金额:58.00 万元
- 项目类别:面上项目
帽结合蛋白(cap binding protein)调控乙烯信号转导的分子机制
- 批准号:
- 批准年份:2021
- 资助金额:58 万元
- 项目类别:
ID1 (Inhibitor of DNA binding 1) 在口蹄疫病毒感染中作用机制的研究
- 批准号:31672538
- 批准年份:2016
- 资助金额:62.0 万元
- 项目类别:面上项目
番茄EIN3-binding F-box蛋白2超表达诱导单性结实和果实成熟异常的机制研究
- 批准号:31372080
- 批准年份:2013
- 资助金额:80.0 万元
- 项目类别:面上项目
P53 binding protein 1 调控乳腺癌进展转移及化疗敏感性的机制研究
- 批准号:81172529
- 批准年份:2011
- 资助金额:58.0 万元
- 项目类别:面上项目
DBP(Vitamin D Binding Protein)在多发性硬化中的作用和相关机制的蛋白质组学研究
- 批准号:81070952
- 批准年份:2010
- 资助金额:35.0 万元
- 项目类别:面上项目
研究EB1(End-Binding protein 1)的癌基因特性及作用机制
- 批准号:30672361
- 批准年份:2006
- 资助金额:24.0 万元
- 项目类别:面上项目
相似海外基金
I-Corps: Translation Potential of Real-time, Ultrasensitive Electrical Transduction of Biological Binding Events for Pathogen and Disease Detection
I-Corps:生物结合事件的实时、超灵敏电转导在病原体和疾病检测中的转化潜力
- 批准号:
2419915 - 财政年份:2024
- 资助金额:
$ 36.35万 - 项目类别:
Standard Grant
Modelling drug binding to biological ion channels
模拟药物与生物离子通道的结合
- 批准号:
2747257 - 财政年份:2022
- 资助金额:
$ 36.35万 - 项目类别:
Studentship
Elucidation of biological functions of the NCBP3 RNA-binding protein using a novel mutant mouse strain
使用新型突变小鼠品系阐明 NCBP3 RNA 结合蛋白的生物学功能
- 批准号:
22K06065 - 财政年份:2022
- 资助金额:
$ 36.35万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
Identifying binding partners, biological substrates and antisense oligonucleotides regulating expression of short and long ACE2.
识别调节短和长 ACE2 表达的结合伴侣、生物底物和反义寡核苷酸。
- 批准号:
BB/V019848/1 - 财政年份:2021
- 资助金额:
$ 36.35万 - 项目类别:
Research Grant
Structure and function of pufferfish toxin, tetrodotoxin, binding proteins as biological defense agent
河豚毒素、河豚毒素、结合蛋白作为生物防御剂的结构和功能
- 批准号:
19K06241 - 财政年份:2019
- 资助金额:
$ 36.35万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
Investigating a biological specificity conundrum: the role of dynamics in transcription factor binding
研究生物特异性难题:动力学在转录因子结合中的作用
- 批准号:
406750 - 财政年份:2018
- 资助金额:
$ 36.35万 - 项目类别:
Studentship Programs
The molecular and biological roles of growth inhibiting chromatin binding proteins
生长抑制染色质结合蛋白的分子和生物学作用
- 批准号:
nhmrc : GNT1143612 - 财政年份:2018
- 资助金额:
$ 36.35万 - 项目类别:
Project Grants
Biological effect and preventive method for human serum albumin binding to transboundary air borne PM2.5.
人血清白蛋白与跨境空气PM2.5结合的生物学效应及预防方法。
- 批准号:
18H03039 - 财政年份:2018
- 资助金额:
$ 36.35万 - 项目类别:
Grant-in-Aid for Scientific Research (B)
The molecular and biological roles of growth inhibiting chromatin binding proteins
生长抑制染色质结合蛋白的分子和生物学作用
- 批准号:
nhmrc : 1143612 - 财政年份:2018
- 资助金额:
$ 36.35万 - 项目类别:
Project Grants
Electrical Detection of Small Molecule Binding to Biological Receptors using Organic Thin Film Transistors : A new approach for label free assays
使用有机薄膜晶体管对小分子与生物受体结合的电检测:一种无标记测定的新方法
- 批准号:
133593 - 财政年份:2018
- 资助金额:
$ 36.35万 - 项目类别:
Feasibility Studies