1 H β chemical shift-based phase modulated NMR methods for fast identification of amino acid types in proteins

被引:0
|
作者
Gartia, Janeka [1 ]
Barnwal, Ravi Pratap [2 ]
机构
[1] Kalinga Inst Ind Technol, Sch Biotechnol, Bhubaneswar 751024, India
[2] Panjab Univ, Dept Biophys, Chandigarh 160014, India
关键词
COUPLING-CONSTANTS; ASSIGNMENTS; RESOLUTION; THREONINE; RESIDUES; PULSES; DOMAIN; MUSIC; N-15;
D O I
10.1016/j.bbrc.2024.150000
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Here we report two phase modulated NMR experiments: PM-2D HN(CACBHB) HB ) and PM-2D HN(HB), HB ), that use 1 H beta chemical shifts to rapidly identify amino acid type in proteins. The magnetization on the 1 H beta spins during the experiments is allowed to evolve for a fixed evolution period that results in phase modulation (positive or negative) of the cross peaks corresponding to various amino acid residues on their 2D HN projections, resembling a typical 2D [1H-15N]-HSQC 1 H- 15 N]-HSQC spectrum. All amino acids except glycine can be categorized into three discernible groups based on their 1 H beta chemical shifts, resulting in unique phase patterns at different fixed evolution periods for 1 H beta , thus facilitating their identification. Remarkably, the PM-2D HN(HB) HB ) stands out among all amino acid type identification NMR techniques for its applicability with cost-effective and most routinely employed 15 N-labeled protein samples for NMR studies. Furthermore, when combined effectively with the 13C beta C beta chemical shift-based phase modulated NMR method (PM-2D HN(CACB)), CB )), these methods resolved the identification of large groups of amino acids into relatively smaller groups. Moreover, these techniques can accelerate the sequence-specific sequential resonance assignment (SSRA) process and would help in fast tracking of assigned NMR signals exhibiting chemical shift perturbation on the 2D [1H-15N]-HSQC 1 H- 15 N]-HSQC spectrum of proteins during various experiments (e.g., temperature change, pH change, and protein or ligand or cofactor binding) as well as in site-directed mutagenesis.
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页数:6
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