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相关概念视频

Structural Protein Function01:56

Structural Protein Function

27.7K
Structural proteins are a category of proteins responsible for functions ranging from cell shape and movement to providing support to major structures such as bones, cartilage, hair, and muscles. This group includes proteins such as collagen, actin, myosin, and keratin.
Collagen, the most abundant protein in mammals, is found throughout the body. In connective tissue, such as skin, ligaments, and tendons, it provides tensile strength and elasticity.  In bones and teeth, it mineralizes to...
27.7K
Fibril-associated Collagen01:11

Fibril-associated Collagen

2.5K
Fibril-associated collagens are a type of collagens present in the extracellular matrix with interrupted triple helices or FACIT (Fibril-associated collagens interrupted triple-helices). FACIT help connect and attach the collagen fibrils with each other as well as with other proteins of the extracellular matrix.
For example, the type II collagen fibrils in cartilage have covalently bound type IX fibril-associated collagens at regular intervals. Other types of fibril-associated collagens are...
2.5K
Type IV Collagen of Basal Lamina01:05

Type IV Collagen of Basal Lamina

2.2K
Type IV collagen is a 400 nm long, network-forming collagen that acts as a barrier between the epithelial and endothelial cells. Type IV collagen  forms the backbone of the basement membrane by scaffolding with laminin, entactin, proteoglycans, and fibronectin. Apart from rendering structural support to the basement membrane, it also helps entail signaling potentials necessary for both pathological and physiological functions.
A type IV collagen molecule has six alpha chains which can...
2.2K
Selectins01:25

Selectins

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Cell adhesion is  an essential aspect of multicellularity. While stable cell interactions usually occur between cells of the same type, transient cell interactions occur between cells of different tissue types, such as between neutrophils and endothelial cells. Selectins are one class of cell adhesion molecules (CAMs) that bind carbohydrate ligands to form transient cell adhesion. They are rod-like proteins with a long extracellular part of variable length ending with the lectin domain,...
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Assembly of Cytoskeletal Filaments01:18

Assembly of Cytoskeletal Filaments

20.0K
Cytoskeletal filaments are polymeric forms of smaller protein subunits. However, individual cytoskeletal filaments may easily disassemble or associate with other similar filaments to form rigid structures. Microfilaments, made of actin monomers, rely on actin-binding proteins to form bundles and create networks of individual actin filaments. Microtubules rely on microtubule-associated proteins (MAPs) to form sturdy cylindrical structures. However, the proteins involved in forming complex...
20.0K
Structure of Cadherins01:25

Structure of Cadherins

3.3K
The cadherins were one of the first cell adhesion molecules discovered; the term “cadherins”   is based on their calcium-dependent adhering properties. The first cadherins discovered on the epithelial, neuronal, and placental cells were named E-cadherin, P-cadherin, and N-cadherin, respectively. These classical cadherins share sequence and structural similarities. Other cadherins, including those involved in cell signaling, are grouped into non-classical cadherins. This...
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相关实验视频

Updated: Jul 6, 2025

In vitro Synthesis of Native, Fibrous Long Spacing and Segmental Long Spacing Collagen
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In vitro Synthesis of Native, Fibrous Long Spacing and Segmental Long Spacing Collagen

Published on: September 20, 2012

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自行分类的原异构体

Valdrin Islami1, Philipp Bittner1, Tomas Fiala1

  • 1Laboratory of Organic Chemistry, ETH Zurich, D-CHAB, Vladimir-Prelog-Weg 3, 8093 Zurich, Switzerland.

Journal of the American Chemical Society
|December 29, 2023
PubMed
概括

科学家们设计出合成原异构体, 这种蛋白质组合代码控制了多个链的分类,证明了对复杂蛋白质结构的精确控制.

科学领域:

  • 生物化学
  • 材料科学
  • 合成生物学

背景情况:

  • 大自然采用复杂的机制来调节蛋白质的组合,特别是在异体原体中.
  • 了解和复制这些自然过程对于开发新生物材料和治疗蛋白质至关重要.

研究的目的:

  • 建立合成原异构体的组成和选择性组装的设计原则.
  • 展示可编程的"组装代码"来控制特定蛋白质结构的形成.

主要方法:

  • 使用补充 (4S) - 氨基和酸盐残留物来直接进行链相互作用.
  • 设计了八种不同的链, 具有特定的序列来促进自我组装.
  • 使用原生电子喷射电离质谱法 (原生ESI-MS) 来分析组装的结构.

主要成果:

  • 成功建立了合成原异构组件的设计原则.
  • 从512个理论组合中证明了八个不同的线程的自我排序成三个特定的三环结构.
  • 原生ESI-MS证实了共存异构体的精确和特定形成.

结论:

  • 开发的"组装代码"为高特异性的蛋白质自组编程提供了强大的工具.

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  • 这项工作为创建可预测结果的定制蛋白质结构奠定了基础.
  • 突出合成生物学方法在设计复杂的生物分子中的潜力.