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関連する概念動画

Hemoglobin01:24

Hemoglobin

9.4K
Hemoglobin is a globular protein made up of four subunits. Two of these subunits are alpha chains, and the other two are beta chains. Each subunit contains a molecule of heme, which has an iron atom and can bind to oxygen. When an oxygen molecule binds to one heme group, it changes the shape of hemoglobin, making it easier for the other heme groups to bind oxygen as well.
When all four heme groups are bound to oxygen, the resulting molecule is called oxyhemoglobin. As a result, arterial blood...
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Oxygen Transport in the Blood01:27

Oxygen Transport in the Blood

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Hemoglobin (Hb) is a crucial molecule in the human body, consisting of four polypeptide chains, each bound to an iron-containing heme group. This unique structure enables hemoglobin to bind to oxygen, with each molecule capable of combining with four molecules of oxygen, leading to rapid and reversible oxygen loading. When fully loaded with oxygen, it is called oxyhemoglobin, while hemoglobin that has released oxygen is called reduced hemoglobin or deoxyhemoglobin. As hemoglobin binds oxygen,...
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Cooperative Allosteric Transitions01:58

Cooperative Allosteric Transitions

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Cooperative allosteric transitions can occur in multimeric proteins, where each subunit of the protein has its own ligand-binding site. When a ligand binds to any of these subunits, it triggers a conformational change that affects the binding sites in the other subunits; this can change the affinity of the other sites for their respective ligands. The ability of the protein to change the shape of its binding site is attributed to the presence of a mix of flexible and stable segments in the...
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Multiple Allele Traits01:49

Multiple Allele Traits

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The Concept of Multiple Allelism
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Gene Families01:57

Gene Families

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Gene families consist of groups of genes proposed to have originated from a common ancestor. Typically these arise through events in which a gene or genes are mistakenly duplicated during cell division. Unlike their parent genes (which are subject to selection pressure to maintain function), these gene copies do not need to preserve their sequences and may evolve at a relatively faster rate.
Occasionally these regions can be adapted to take on new roles within the organism, becoming novel genes...
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Protein Families02:47

Protein Families

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Protein families are groups of homologous proteins; that is, they have similarities in amino acid sequences and three-dimensional structures. Protein families usually occur because of gene duplication, where an additional copy of a gene is inserted into the genome of an organism.   Mutations that change the amino acids but still allow the protein to be properly synthesized, will lead to new protein family members.   If these new proteins contain similar amino acids in key...
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Updated: Mar 12, 2026

A Precision Medicine Tool for Measurement and Monitoring of Hemoglobin S in Sickle Cell Disease Patients Receiving Transfusion Therapy
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A Precision Medicine Tool for Measurement and Monitoring of Hemoglobin S in Sickle Cell Disease Patients Receiving Transfusion Therapy

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ヘモグロビン 機能 の 予測 できる 収束 は,予測 でき ない 分子 基盤 を 持つ

Chandrasekhar Natarajan1, Federico G Hoffmann2, Roy E Weber3

  • 1School of Biological Sciences, University of Nebraska, Lincoln, NE 68588, USA.

Science (New York, N.Y.)
|November 16, 2016
PubMed
まとめ
この要約は機械生成です。

遺伝的適応は 予測可能な機能的変化を示しますが 予測できない分子根源です 歴史的変異と遺伝的背景は 進化の経路を制限するので 適応的な解決策は種間で普遍的ではありません

さらに関連する動画

Measuring Deformability and Red Cell Heterogeneity in Blood by Ektacytometry
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Measuring Deformability and Red Cell Heterogeneity in Blood by Ektacytometry

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Characterization of Sickling During Controlled Automated Deoxygenation with Oxygen Gradient Ektacytometry
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Characterization of Sickling During Controlled Automated Deoxygenation with Oxygen Gradient Ektacytometry

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関連する実験動画

Last Updated: Mar 12, 2026

A Precision Medicine Tool for Measurement and Monitoring of Hemoglobin S in Sickle Cell Disease Patients Receiving Transfusion Therapy
07:24

A Precision Medicine Tool for Measurement and Monitoring of Hemoglobin S in Sickle Cell Disease Patients Receiving Transfusion Therapy

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Measuring Deformability and Red Cell Heterogeneity in Blood by Ektacytometry
09:12

Measuring Deformability and Red Cell Heterogeneity in Blood by Ektacytometry

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Characterization of Sickling During Controlled Automated Deoxygenation with Oxygen Gradient Ektacytometry
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Characterization of Sickling During Controlled Automated Deoxygenation with Oxygen Gradient Ektacytometry

Published on: November 5, 2019

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科学分野:

  • 進化生物学
  • 分子進化
  • 生物化学

背景:

  • 遺伝的適応は 進化的変化を促します
  • ヘモグロビンと酸素の親和性は 高地での生存に不可欠です
  • 進化の予測可能性が明らかになるのです

研究 の 目的:

  • 遺伝的適応の予測可能性を調査する
  • 収束性ヘモグロビン機能の進化の分子基礎を検証する.
  • 適応における歴史的偶然性の役割を評価する.

主な方法:

  • 標高が異なる56種の鳥類を比較分析した.
  • ヘモグロビンのアミノ酸置換分析
  • 復活した祖先のタンパク質の実験

主要な成果:

  • ヘモグロビンと酸素の相性における収束的増加は,高海拔の鳥の間で一般的であった.
  • パラレルアミノ酸の置換により,収束した機能的変化は少なかった.
  • 歴史的な置換は,タンパク質の機能に文脈に依存した効果を持っていた.
  • 遺伝的背景は変異の適応力に影響した.

結論:

  • 生物化学的表型は 予測可能な適応を示します
  • 適応の分子の基礎は 常に予測できるものではありません
  • 進化的適応は歴史的偶然性や 遺伝的背景によって制約されています