Non-covalent halotag ligands
AssigneeMax-Planck-Gesellschaft Zur FöRderung Der Wissenschaften E. V.
InventorsKai JOHNSSON, Julien HIBLOT, Julian KOMPA
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AssigneeMax-Planck-Gesellschaft Zur FöRderung Der Wissenschaften E. V.
InventorsKai JOHNSSON, Julien HIBLOT, Julian KOMPA
Estimating the term…
A first aspect of the invention relates to a non-covalently-HaloTag-binding compound characterized by the general formula D-L-T (I), wherein D is or comprises a functional moiety Z, particularly a fluorescent dye, or D is a linkable moiety (i.e. a moiety that can be coupled to other functional groups), L is a linear linker of 10-15 atoms in length, and T is a moiety selected from the group comprising methylamine, methylsulfonamide, acetamide, or their respective fluorinated analogues, azide, or hydroxyl. Another aspect of the invention relates to a HaloTag variant wherein position D106 of the HaloTag7 sequence is exchanged for a proteinogenic amino acid different from D. The variant has a different binding specificity for HaloTag substrates compared to the non-variant Halotag polypeptide. Yet another aspect of the invention relates to kits comprising polypeptides or nucleic acids and the non-covalently-HaloTag-binding compound according to the invention.
A non-covalently-HaloTag-binding compound characterized by the general formula (I)
A non-covalently-HaloTag-binding compound characterized by the general formula (I)
A D106 mutant HaloTag polypeptide, wherein, in a HaloTag7 polypeptide sequence or a HaloTag polypeptide sequence homologous to HaloTag7, at position D106 of HaloTag7 or at a position homologous to D106 of HaloTag7, D is exchanged for a proteinogenic amino acid different from D,
Dependencies are inferred from the claim text.