摘要:
The present invention includes compositions and methods for treating a subject with a G protein coupled receptors (GPCRs) misfolded, misrouted, or both misfolded and misrouted protein comprising: obtaining a sample from the subject suspected of having a G protein coupled receptor (GPCR) that is misfolded, misrouted, or both misfolded and misrouted; and providing the subject with an effective amount of a pharmacoperone that prevents misfolding, misrouting, or both misfolding and misrouting of the GPCR protein.
摘要:
Disclosed is the use of latrophilin expression as a biomarker for the diagnosis of haematopoietic cell cancer in a subject, together with methods for diagnosis and a kit for the detection of latrophilin expression on white blood cells collected from a subject.
摘要:
The disclosure provides novel methods of determining or comparing potency of a test interferon relative to rSIFN-co (an interferon having therapeutic effects on solid tumors); methods of establishing substantial equivalence between a test interferon and rSIFN-co; as well as methods for determining potency of a test interferon, kits for determining such methods, and an interferon or an interferon substitute having said activities.
摘要:
The present invention relates to a compound of formula (I), wherein R is defined as in the description and in the claims. The compound of formula (I) can be used as radiolabeled ligand.
摘要:
Resonance energy transfer (RET)- or protein-fragment complement assay (PCA)- based biosensors useful for assessing the activity of G-proteins are described. These biosensors are based on the competition between the Gα subunit and a Gβγ interacting protein (βγ IP) for the binding to the Gβγ dimer. These biosensors comprises (1) a βγ IP and (2) a Gβ or Gγ protein; a GPCR; or a plasma membrane targeting domain, fused to suitable RET or PCA tags. Methods using such biosensors for different applications, including the identification of agents that modulates G-protein activity or for the characterization of GPCR signaling/regulation, such as G-protein preferences and activation profiles of GPCRs, are also described.
摘要:
029P-GFR-WO01 42 ABSTRACT Disclosed herein are cell lines transformed to express G-Protein Coupled Receptor GPCR22 and uses thereof for identifying guanosine analogues and/or other ligands to the receptor. In particular, techniques for transforming Drosophila Schneider 2 cells and human astrocytoma 1321N1 cell to express GPCR22 are disclosed as well as transformed cells lines. The transformed cell lines of the instant disclosure may be useful in identifying guanosine analogues and functional equivalents thereof.
摘要:
The present invention relates to pharmaceutical compositions for use in a method of treatment of ventilator-induced diaphragmatic dysfunction. In particular, the present invention relates to a therapeutically effective amount of a beta2-adrenergic receptor antagonist for use in a method for the treatment of ventilator-induced diaphragmatic dysfunction in a subject in need thereof.
摘要:
The present invention relates to methods and pharmaceutical compositions for the treatment of hepatocellular carcinomas. In particular, the present invention relates to an OX1R agonist for use in the treatment of hepatocellular carcinomain a subject in need thereof.
摘要:
본 발명은 이종이합체 G 단백질 연결 수용체를 포함하는 나노베지클, 이의 제조 방법 및 이를 포함하는 전계효과 트랜지스터 기반 미각 센서, 이의 제조 방법에 관한 것이다. 본 발명에 따른 이종이합체 G 단백질 연결 수용체를 포함하는 나노베지클로 기능화된 전계효과 트랜지스터 및 미각 센서는 이종이합체 G 단백질 연결 수용체 및 이를 포함하는 나노베지클을 이용하여, 민감도 및 선택도가 우수하고 실시간으로 고특이적으로 단맛 물질을 검출할 수 있다.
摘要:
Provided herein are recombinant virion arrays comprising human membrane bound proteins that retain their native conformations and/or interactions, recombinant HSV-1 virions, and methods of use including high-content, high-throughput assays for screening for ligands and/or drugs that bind human membrane bound proteins, diagnostic assays, proteomic assays, and biosensor assays. Also provided are recombinant HSV-1 virions comprising an envelope comprising a plurality of heterologous membrane bound proteins that retain their native conformations and/or interactions as well as recombinant HSV-1 bacterial artificial chromosome (BAC) clones encoding heterologous membrane polypeptides.