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    • 3. 发明授权
    • Method of using G-matrix fourier transformation nuclear magnetic resonance (GFT NMR) spectroscopy for rapid chemical shift assignment and secondary structure determination of proteins
    • 使用G矩阵傅里叶变换核磁共振(GFT NMR)光谱法进行蛋白质快速化学位移分配和二级结构测定的方法
    • US07880468B2
    • 2011-02-01
    • US12057076
    • 2008-03-27
    • Thomas A. SzyperskiSeho KimHanudatta S. Atreya
    • Thomas A. SzyperskiSeho KimHanudatta S. Atreya
    • G01V3/00
    • G01R33/4633G01R33/465Y10T436/24
    • The present invention presents a new approach to rapidly obtaining precise high-dimensional NMR spectral information, named “GFT NMR spectroscopy”, which is based on the phase sensitive joint sampling of the indirect dimensions spanning a subspace of a conventional NMR experiment. The phase-sensitive joint sampling of several indirect dimensions of a high-dimensional NMR experiment leads to largely reduced minimum measurement times when compared to FT NMR. This allows one to avoid the “sampling limited” data collection regime. Concomitantly, the analysis of the resulting chemical shift multiplets, which are edited by the G-matrix transformation, yields increased precision for the measurement of the chemical shifts. Additionally, methods of conducting specific GFT NMR experiments as well as methods of conducting a combination of GFT NMR experiments for rapidly obtaining precise chemical shift assignment and determining the structure of proteins or other molecules are disclosed.
    • 本发明提供了一种快速获得精确的高维NMR光谱信息的新方法,命名为“GFT NMR光谱”,其基于跨过常规NMR实验的子空间的间接尺寸的相敏联合采样。 与FT NMR相比,高维NMR实验的几个间接尺寸的相敏联合取样导致最大测量时间大大降低。 这样可以避免“采样受限”的数据收集制度。 伴随地,通过G矩阵变换编辑的所得到的化学位移多重峰的分析产生了用于测量化学位移的增加的精度。 此外,公开了进行特定GFT NMR实验的方法以及进行GFT NMR实验的组合以快速获得精确的化学位移分配和确定蛋白质或其他分子的结构的方法。
    • 5. 发明授权
    • Method of using G-matrix fourier transformation nuclear magnetic resonance (GFT NMR) spectroscopy for rapid chemical shift assignment and secondary structure determination of proteins
    • 使用G矩阵傅里叶变换核磁共振(GFT NMR)光谱法进行蛋白质快速化学位移分配和二级结构测定的方法
    • US07365539B2
    • 2008-04-29
    • US10973807
    • 2004-10-26
    • Thomas A. SzyperskiSeho KimHanudatta S. Atreya
    • Thomas A. SzyperskiSeho KimHanudatta S. Atreya
    • G01V3/00
    • G01R33/4633G01R33/465Y10T436/24
    • The present invention presents a new approach to rapidly obtaining precise high-dimensional NMR spectral information, named “GFT NMR spectroscopy”, which is based on the phase sensitive joint sampling of the indirect dimensions spanning a subspace of a conventional NMR experiment. The phase-sensitive joint sampling of several indirect dimensions of a high-dimensional NMR experiment leads to largely reduced minimum measurement times when compared to FT NMR. This allows one to avoid the “sampling limited” data collection regime. Concomitantly, the analysis of the resulting checmical shift multiplets, which are edited by the G-matrix transformation, yields increased precision for the measurement of the chemical shifts. Additionally, methods of conducting specific GFT NMR experiments as well as methods of conducting a combination of GFT NMR experiments for rapidly obtaining precise chemical shift assignment and determining the structure of proteins or other molecules are disclosed.
    • 本发明提出了一种快速获得精确的高维NMR光谱信息的新方法,命名为“GFT NMR光谱”,其基于跨过常规NMR实验的子空间的间接尺寸的相敏联合采样。 与FT NMR相比,高维NMR实验的几个间接尺寸的相敏联合取样导致最大测量时间大大降低。 这样可以避免“采样受限”的数据收集制度。 伴随地,通过G矩阵变换编辑的所得到的移动多重点的分析产生了用于化学位移测量的增加的精度。 此外,公开了进行特定GFT NMR实验的方法以及进行GFT NMR实验的组合以快速获得精确的化学位移分配和确定蛋白质或其他分子的结构的方法。
    • 6. 发明授权
    • Method of using reduced dimensionality nuclear magnetic resonance spectroscopy for rapid chemical shift assignment and secondary structure determination of proteins
    • 使用降低维数的核磁共振光谱法进行蛋白质快速化学位移分配和二级结构测定的方法
    • US07141432B2
    • 2006-11-28
    • US09897583
    • 2001-06-29
    • Thomas A. Szyperski
    • Thomas A. Szyperski
    • G01N24/00G01N33/00
    • G01R33/4625G01R33/4608G01R33/4633G01R33/465Y10T436/24
    • The present invention discloses eight new reduced dimensionality (RD) triple resonance nuclear magnetic resonance (NMR) experiments for measuring chemical shift values of certain nuclei in a protein molecule. The RD 3D HA,CA,(CO),N,HN NMR experiment and the RD 3D H,C,(C-TOCSY—CO),N,HN NMR experiment are designed to yield “sequential” connectivities, while the RD 3D Hαβ,Cαβ,CO,HA NMR experiment and the RD 3D Hαβ,Cαβ,N,HN NMR experiment provide “intraresidue” connectivities. The RD 3D H,C,C,H—COSY NMR experiment, the RD 3D H,C,C,H-TOCSY NMR experiment, and the RD 2D H,C,H—COSY NMR experiment allow one to obtain assignments for aliphatic and aromatic side chain chemical shifts, while the RD 2D HB,CB,(CG,CD),HD NMR experiment provide information for the aromatic side chain chemical shifts. In addition, a method of conducting suites of RD triple resonance NMR experiments for high-throughput resonance assignment of proteins and identification of the location of secondary structure elements are disclosed.
    • 本发明公开了用于测量蛋白质分子中某些核的化学位移值的八个新的降维(RD)三重共振核磁共振(NMR)实验。 CA,(CO),N,HN NMR实验和RD 3D H, H, H alphabeta CO,HA NMR实验和RD 3D H字母表 H, C,C,H-COZY NMR实验,RD 3D H, H, C,H-COZY NMR实验允许一个获得脂族和芳族 侧链化学位移,而RD 2D HB,(UC,CD),HD NMR实验提供了芳族侧链化学位移的信息。 另外,公开了用于蛋白质高通量共振分配的RD三重共振NMR实验套件的方法和二级结构元件的位置的识别。
    • 7. 发明授权
    • Phase sensitively-detected reduced dimensionality nuclear magnetic resonance spectroscopy for rapid chemical shift assignment and secondary structure determination of proteins
    • 相位敏感检测降低维度核磁共振波谱用于蛋白质的快速化学位移分配和二级结构测定
    • US07396685B2
    • 2008-07-08
    • US10628818
    • 2003-07-28
    • Thomas A. SzyperskiSeho Kim
    • Thomas A. SzyperskiSeho Kim
    • G01N24/00
    • G01R33/4633G01R33/465Y10T436/24
    • The present invention discloses eleven reduced dimensionality (RD) triple resonance nuclear magnetic resonance (NMR) experiments for measuring chemical shift values of certain nuclei in a protein molecule, where the chemical shift values encoded in a peak pair of an NMR spectrum are detected in a phase sensitive manner. The RD 3D HA,CA,(CO),N,HN NMR and RD 3D H,C,(C-TOCSY-CO),N,HN NMR experiments are designed to yield “sequential” connectivities, while the RD 3D Hα/β,Cα/β,CO,HA NMR and RD 3D Hα/β,Cα/β,N,HN NMR experiments provide “intraresidue” connectivities. The RD 3D H,C,C,H-COSY NMR, RD 3D H,C,C,H-TOCSY NMR, and RD 2D H,C,H-COSY NMR experiments allow one to obtain assignments for aliphatic and aromatic side chain chemical shifts, while the RD 2D HB,CB,(CG,CD),HD NMR experiment provide information for the aromatic side chain chemical shifts. In addition, methods of conducting suites of RD triple resonance NMR experiments for high-throughput resonance assignment of proteins and determination of secondary structure elements are disclosed.
    • 本发明公开了一种用于测量蛋白质分子中某些核的化学位移值的十一维三维共振核磁共振(NMR)实验,其中在一个核磁共振谱的峰对中编码的化学位移值在 相位敏感的方式。 CA,(CO),N,HN NMR和RD 3D H, Hα/β, CO,HA NMR和RD 3D Hα/β, N,1 H NMR实验提供“残留”连接。 C,C,H-COZY NMR,RD 3D H, H, C,C,H-TOCSY NMR和RD 2D H, HB,(UC,CD),HD NMR实验提供了芳族侧链化学位移的信息。 此外,公开了用于蛋白质的高通量共振分配的RD三重共振NMR实验的套件的方法和二级结构元件的测定。
    • 8. 发明申请
    • PHASE-SENSITIVELY DETECTED REDUCED DIMENSIONALITY NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY FOR RAPID CHEMICAL SHIFT ASSIGNMENT AND SECONDARY STRUCTURE DETERMINATION OF PROTEINS
    • 相敏检测减少尺寸核激光共振光谱快速化学转移分配和二级结构测定蛋白质
    • US20090115414A1
    • 2009-05-07
    • US12132320
    • 2008-06-03
    • Thomas A. SzyperskiSeho Kim
    • Thomas A. SzyperskiSeho Kim
    • G01R33/44
    • G01R33/4633G01R33/465Y10T436/24
    • The present invention discloses eleven reduced dimensionality (RD) triple resonance nuclear magnetic resonance (NMR) experiments for measuring chemical shift values of certain nuclei in a protein molecule, where the chemical shift values encoded in a peak pair of an NMR spectrum are detected in a phase sensitive manner. The RD 3D HA,CA,(CO),N,HN NMR and RD 3D H,C,(C-TOCSY-CO),N,HN NMR experiments are designed to yield “sequential” connectivities, while the RD 3D Hα/β,Cα/β, CO,HA NMR and RD 3D Hα/β,Cα/β,N,HN NMR experiments provide “intraresidue” connectivities. The RD 3D H,C,C,H-COSY NMR, RD 3D H,C,C,H-TOCSY NMR, and RD 2D H,C,H-COSY NMR experiments allow one to obtain assignments for aliphatic and aromatic side chain chemical shifts, while the RD 2D HB,CB,(CG,CD),HD NMR experiment provide information for the aromatic side chain chemical shifts. In addition, methods of conducting suites of RD triple resonance NMR experiments for high-throughput resonance assignment of proteins and determination of secondary structure elements are disclosed.
    • 本发明公开了一种用于测量蛋白质分子中某些核的化学位移值的十一维三维共振核磁共振(NMR)实验,其中在一个核磁共振谱的峰对中编码的化学位移值在 相位敏感的方式。 HA,CA,(CO),N,HN NMR和RD 3D H,单独的 “C,(C-TOCSY-CO),N,HN NMR实验被设计为产生”顺序“连接,而RD 3D Hal /β, Calpha / beta,CO,HA NMR和RD 3D氦/氦,Calpha /β,N,HN NMR实验提供了“残留”连接。 RD 3D H,C,C,H-COZY NMR,RD 3D,H, C,C,H-TOCSY NMR和RD 2D H,C,H-COZY NMR实验允许获得脂族和芳族侧链化学位移的分配 ,而DB 2D,CB,(CG,CD),HD NMR实验提供了芳族侧链化学位移的信息。 此外,公开了用于蛋白质的高通量共振分配的RD三重共振NMR实验的套件的方法和二级结构元件的测定。