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Engineering of a bis-chelator motif into a protein α-helix for rigid lanthanide binding and paramagnetic NMR spectroscopy

机译:将双螯合剂基序工程化为蛋白质α-螺旋,以实现刚性镧系元素结合和顺磁NMR光谱

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摘要

Attachment of two nitrilotriacetic acid-based ligands to a protein a-helix in an i, i + 4 configuration produces an octadentate chelating motif that is able to bind paramagnetic lanthanide ions rigidly and with high affinity, leading to large pseudocontact shifts and residual dipolar couplings in the NMR spectrum.
机译:将两个基于次氮基三乙酸的配体以i,i + 4构型连接到蛋白质a-螺旋上产生八齿螯合基序,该基序能够牢固地并具有高亲和力地结合顺磁性镧系元素离子,从而导致较大的伪接触位移和残留的偶极耦合在NMR光谱中。

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  • 来源
    《Chemical Communications》 |2011年第26期|p.7368-7370|共3页
  • 作者单位

    Medicinal Chemistry and Drug Action, Monash Institute of Pharmaceutical Sciences, Parkville, VIC 3052;

    Medicinal Chemistry and Drug Action, Monash Institute of Pharmaceutical Sciences, Parkville, VIC 3052;

    Research School of Chemistry, Australian National University, Canberra, ACT 0200;

    Research School of Chemistry, Australian National University, Canberra, ACT 0200 ,Latvian Institute of Organic Synthesis, Riga, LV-1006, Latvia;

    Medicinal Chemistry and Drug Action, Monash Institute of Pharmaceutical Sciences, Parkville, VIC 3052;

    Research School of Chemistry, Australian National University, Canberra, ACT 0200;

    Research School of Chemistry, Australian National University, Canberra, ACT 0200;

    Medicinal Chemistry and Drug Action, Monash Institute of Pharmaceutical Sciences, Parkville, VIC 3052;

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  • 入库时间 2022-08-17 13:22:32

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