摘要:
The present disclosure provides albumin conjugates for the treatment of cancer, and more particularly conjugates of albumin with 7-ethyl-10-hydroxy-camptothecin.
摘要:
Example embodiments in accordance with the present disclosure are directed to methods for transforming a Cannabaceae plant part by exposing the Cannabaceae plant part to an expression construct comprising a nucleotide sequence encoding an albumin to transform the Cannabaceae plant part with the expression construct, and inducing production of the albumin in the transformed Cannabaceae plant part.
摘要:
The present disclosure generally relates to novel Tregitope-blood component conjugates and modified polypeptides comprising Tregitopes, with said modified peptides being capable of reacting with blood components to form such Tregitope-blood component conjugates. In aspects, the Tregitope-blood component conjugates include a blood component which acts as a carrier protein (e.g., albumin), and further include a modified polypeptide comprising one or more regulatory T cell epitopes (termed "Tregitopes"), the polypeptide having been modified by attaching a reactive moiety to the polypeptide that is capable of forming a bond (e.g., a covalent linkage) with a reactive functionality on the blood component. The present disclosure also relates to methods of using said Tregitope-blood component conjugates and modified polypeptides comprising Tregitopes in the treatment and prevent of autoimmune disorders, such as type 1 diabetes.
摘要:
The present disclosure provides, in part, a cell culture medium supplement comprising at least one plant protein homologue of a serum protein, a cell culture medium comprising a serum-free base medium and one or more plant based proteins, and methods of growing cells in vitro and of producing cultured meat using the cell culture medium.
摘要:
The present disclosure relates to protein sequences which can be used to generate factor Xa proteins and derivatives thereof. The protein sequences include a factor Xa light chain portion, a heavy chain catalytic domain portion, and an activation peptide C-terminal to the heavy chain catalytic domain portion. It is discovered that when an activation peptide (AP) is fused to the C-terminal end of the heavy chain of the factor Xa protein or derivative, the resulting protein can be more efficiently expressed, and the attachment of the activation peptide (AP) to the heavy chain does not affect the activity of the protein.
摘要:
Provided herein are methods of generating MDSCs ex vivo. The methods include culturing blood cells with an LRP2 agonist. The method includes upregulating or expressing LRP2 on blood cells and culturing the blood cells with lactoferrin. In one embodiment, the blood cells are selected from peripheral blood mononuclear cells, cord blood, and bone marrow cells.
摘要:
Contemplated compositions and methods comprise chimeric molecule complexes that advantageously provide activating signaling to immune competent cells when bound to ALL cells. Furthermore, chimeric molecule complexes include an Fc portion to extend serum half live time and facilitate purification.
摘要:
A non-covalent complex of an albumin molecule and a hydrophobic ligand, compositions containing the same, and methods of use thereof are provided. The present complex may find use in delivering the hydrophobic ligand to microorganisms that have albumin-binding outer surfaces, such as a cell wall.
摘要:
The present invention relates to a fusion protein comprising albumin and a retinol-binding protein, which is useful in preventing or treating fibrotic diseases. The fusion protein, in which albumin and a retinol-binding protein (RBP) are bound together, induces the formation of cytoplasmic lipid droplets in stellate cells and returns the shape of activated stellate cells to the previous shape thereof before activation. Therefore, the fusion protein of the present invention may be effectively used in preventing or treating fibrotic diseases occurring in liver, pancreas, lungs, or the like.