While residual dipolar couplings (RDCs) are an established method in high-resolution biomolecular
NMR, their use for structure determination of small molecules in organic solvents is limited by the alignment
media available. Only recently stretched polystyrene (PS) gels were introduced for the measurement of
RDCs on small compounds that allowed urgently needed free scalability of the induced anisotropy. Here,
the properties of such stretched PS gels in different organic solvents as well as for different magnetic field
strengths and temperatures are studied and practical NMR-spectroscopic aspects are discussed.
Residual dipolar couplings (RDCs) have revolutionized the NMR-based structure determination of large biomolecules [1][2][3][4] and lately demonstrated their potential in the field of small molecules. [5][6][7][8][9][10][11][12] The measurement of RDCs relies on the partial orientation of the molecule of interest, for which a socalled alignment medium is necessary. In aqueous solution a variety of alignment media are known, for example,[*] Dr.
A convenient synthesis of novel bifunctional poly(amino carboxylate) chelating agents allowing chemoselective attachment to highly functionalized biomolecules is described. Based on the well known chelator 1,4,7,10-tetraazacyclodecane-1,4,7,10-tetraacetic acid (DOTA), we synthesized novel bifunctional chelating agents bearing additional functional groups by alkylating 1,4,7,10-tetraazacyclododecane (cyclen) with one equivalent of para-functionalized alkyl 2-bromophenyl-acetate and three equivalents of tert-butyl 2-bromoacetate. The resulting compounds, which contain an additional carbonyl or alkyne functionality, allow site specific labeling of appropriately functionalized unprotected biomolecules in a rapid manner via click reactions. This was demonstrated by the attachment of our new DOTA derivatives to the somatostatin analogue Tyr3-octreotate by chemoselective oxime ligation and CuI-catalyzed azide-alkyne cycloaddition. Initial biodistribution studies in mice with the radiometalated compound demonstrated the applicability of the described DOTA conjugation.
Ovarian cancer cells overexpressing uPAR were specifically targeted in vitro and in vivo by (213)Bi-P-P4D. Kidney uptake of (213)Bi-P-P4D was distinctly reduced using gelofusine. Thus, this radiopeptide may represent a promising option for therapy for disseminated ovarian cancer.
Residual dipolar couplings (RDCs) have revolutionized the NMR-based structure determination of large biomolecules [1][2][3][4] and lately demonstrated their potential in the field of small molecules. [5][6][7][8][9][10][11][12] The measurement of RDCs relies on the partial orientation of the molecule of interest, for which a socalled alignment medium is necessary. In aqueous solution a variety of alignment media are known, for example,[*] Dr.
Perdeuterated poly(styrene) is introduced as an almost artefact-free and arbitrarily scalable alignment medium for measuring residual dipolar couplings and other anisotropic NMR parameters; the spectral quality achievable in this new medium is demonstrated for HSQC spectra leading to the conformational analysis of staurosporine and homonuclear TOCSY-type experiments.
Hemophilia A, one of the most severe bleeding disorders, results from an inherited deficiency of factor VIII (FVIII) function. Treatment by injection of FVIII has been a common procedure for decades. Nevertheless, the production and purification of FVIII remains a challenging task. Current procedures using immunoaffinity chromatography are expensive and suffer from the instability of the applied antibody ligands, which elute along with the product and contaminate it. Recently, FVIII was purified by use of octapeptide ligands, but their low protease-resistance limits their application. We here report the systematic rational and combinatorial optimization procedure that allowed us to transfer the octapeptide ligands into a small peptidomimetic. This compound is the smallest ligand known for separation of such a large protein (330 kDa). It not only binds and purifies FVIII with high efficiency but also is stable, protease-resistant, and cheap to produce in preparative scale. Hence it offers a valuable alternative to antibody-based purification procedures.
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