Acquisition of Octet Biolayer Interferometry system for MIT biophysics facility

为麻省理工学院生物物理设施采购 Octet Biolayer 干涉测量系统

基本信息

项目摘要

PROJECT SUMMARY All living processes are regulated by the dynamic interactions of proteins with small molecule ligands, partner proteins, nucleic acids, or other macromolecules. Instrumentation that enables quantitative analysis of the specificities and avidities of these interactions in vitro provides a physical foundation for understanding the intricate networks of reactions that contribute to complex biological processes. In this proposal, eleven faculty in the Departments of Biology and Biological Engineering at MIT request funding for the acquisition of an Octet RED96 instrument for the analysis of biomolecular interactions. This instrumentation exploits biolayer interferometry (BLI) to provide real time information on the binding of ligands in solution to immobilized molecules. The instrumentation accommodates a 96-well plate format for high- throughput analysis and is exceptionally versatile. Ligands can range from small molecules (>150 Da) up to very large protein or nucleic acid oligomers, and the acquisition of association and dissociation rate constants rapidly provides equilibrium constants over a broad dynamic range (10 pM - 1 mM) with very efficient sample requirements. Community access to hands-on use of this equipment will advance the pace and sophistication of multiple research programs and will be guaranteed by the central location of the instrument in the shared Biophysical Instrumentation Facility (BIF) in Building 68 of the MIT campus, which is run by a full-time technician (Ms. Debby Pheasant) and is directed by Professor Barbara Imperiali. The oversight committee for the acquisition and administration of all equipment in the BIF comprises Professors Barbara Imperiali (Chair), Robert Sauer, Amy E. Keating, Jacquin Niles and Ms. Debby Pheasant. !
项目总结

项目成果

期刊论文数量(11)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
De Novo Discovery of High-Affinity Peptide Binders for the SARS-CoV-2 Spike Protein.
  • DOI:
    10.1021/acscentsci.0c01309
  • 发表时间:
    2021-01-27
  • 期刊:
  • 影响因子:
    18.2
  • 作者:
    Pomplun S;Jbara M;Quartararo AJ;Zhang G;Brown JS;Lee YC;Ye X;Hanna S;Pentelute BL
  • 通讯作者:
    Pentelute BL
Generation of Thermally Stable Affinity Pairs for Sensitive, Specific Immunoassays.
生成热稳定亲和对,用于灵敏、特异性的免疫测定。
  • DOI:
    10.1007/978-1-0716-2285-8_21
  • 发表时间:
    2022
  • 期刊:
  • 影响因子:
    0
  • 作者:
    Corless,Elliot;Hao,Yining;Jia,Huan;Kongsuphol,Patthara;Tay,DousabelMY;Ng,SayYong;Sikes,HadleyD
  • 通讯作者:
    Sikes,HadleyD
Salt Effect Accelerates Site-Selective Cysteine Bioconjugation.
  • DOI:
    10.1021/acscentsci.6b00180
  • 发表时间:
    2016-09-28
  • 期刊:
  • 影响因子:
    18.2
  • 作者:
    Dai, Peng;Zhang, Chi;Welborn, Matthew;Shepherd, James J.;Zhu, Tianyu;Van Voorhis, Troy;Pentelute, Bradley L.
  • 通讯作者:
    Pentelute, Bradley L.
Discovery of Nucleic Acid Binding Molecules from Combinatorial Biohybrid Nucleobase Peptide Libraries.
  • DOI:
    10.1021/jacs.0c08964
  • 发表时间:
    2020-11-18
  • 期刊:
  • 影响因子:
    15
  • 作者:
    Pomplun S;Gates ZP;Zhang G;Quartararo AJ;Pentelute BL
  • 通讯作者:
    Pentelute BL
A reactive peptide interface for site-selective cysteine bioconjugation.
  • DOI:
    10.1039/d1cc00095k
  • 发表时间:
    2021-04-04
  • 期刊:
  • 影响因子:
    0
  • 作者:
    Tuang S ;Dieppa-Matos D ;Zhang C ;Shugrue CR ;Dai P ;Loas A ;Pentelute BL
  • 通讯作者:
    Pentelute BL
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Barbara Imperiali其他文献

Barbara Imperiali的其他文献

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{{ truncateString('Barbara Imperiali', 18)}}的其他基金

Development and application of glycan readers for the detection and analysis of bacterial glycoconjugates
用于细菌糖复合物检测和分析的聚糖读数器的开发和应用
  • 批准号:
    9295172
  • 财政年份:
    2017
  • 资助金额:
    $ 18.04万
  • 项目类别:
PGT Inhibitors Mapped From a Tunicamycin Blueprint
根据衣霉素蓝图绘制的 PGT 抑制剂
  • 批准号:
    8508008
  • 财政年份:
    2013
  • 资助金额:
    $ 18.04万
  • 项目类别:
PGT Inhibitors Mapped From a Tunicamycin Blueprint
根据衣霉素蓝图绘制的 PGT 抑制剂
  • 批准号:
    8607890
  • 财政年份:
    2013
  • 资助金额:
    $ 18.04万
  • 项目类别:
Inhibition of Glycoprotein Biosynthesis in Gram-Negative Pathogens
革兰氏阴性病原体糖蛋白生物合成的抑制
  • 批准号:
    8420337
  • 财政年份:
    2012
  • 资助金额:
    $ 18.04万
  • 项目类别:
Inhibition of Prokaryote-Specific Saccharide Biosynthesis in Microbial Pathogens
微生物病原体中原核生物特异性糖生物合成的抑制
  • 批准号:
    9004701
  • 财政年份:
    2012
  • 资助金额:
    $ 18.04万
  • 项目类别:
Inhibition of prokaryote-specific saccharide biosynthesis in microbial pathogens
微生物病原体中原核生物特异性糖生物合成的抑制
  • 批准号:
    8235459
  • 财政年份:
    2012
  • 资助金额:
    $ 18.04万
  • 项目类别:
Inhibition of Glycoprotein Biosynthesis in Gram-Negative Pathogens
革兰氏阴性病原体糖蛋白生物合成的抑制
  • 批准号:
    8262295
  • 财政年份:
    2012
  • 资助金额:
    $ 18.04万
  • 项目类别:
Inhibition of Prokaryote-Specific Saccharide Biosynthesis in Microbial Pathogens
微生物病原体中原核生物特异性糖生物合成的抑制
  • 批准号:
    8757021
  • 财政年份:
    2012
  • 资助金额:
    $ 18.04万
  • 项目类别:
Inhibition of prokaryote-specific saccharide biosynthesis in microbial pathogens
微生物病原体中原核生物特异性糖生物合成的抑制
  • 批准号:
    8446469
  • 财政年份:
    2012
  • 资助金额:
    $ 18.04万
  • 项目类别:
Inhibition of Prokaryote-Specific Saccharide Biosynthesis in Microbial Pathogens
微生物病原体中原核生物特异性糖生物合成的抑制
  • 批准号:
    9265228
  • 财政年份:
    2012
  • 资助金额:
    $ 18.04万
  • 项目类别:

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新型生物过程中的一氧化二氮管理
  • 批准号:
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    2023
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