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Competitive advantage of diferric transferrin in delivering iron to reticulocytes.脱铁转铁蛋白在将铁传递给网织红细胞方面的竞争优势。
Proc Natl Acad Sci U S A. 1983 Jan;80(1):300-4. doi: 10.1073/pnas.80.1.300.
2
Interaction of human diferric transferrin with reticulocytes.人脱铁转铁蛋白与网织红细胞的相互作用。
Proc Natl Acad Sci U S A. 1981 Jan;78(1):621-5. doi: 10.1073/pnas.78.1.621.
3
Uptake and release of iron from human transferrin.铁从人转铁蛋白中的摄取与释放
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4
The effect of the iron saturation of transferrin on its binding and uptake by rabbit reticulocytes.转铁蛋白的铁饱和度对其与兔网织红细胞结合及被摄取的影响。
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Iron uptake from rat plasma transferrin by rat reticulocytes.大鼠网织红细胞从大鼠血浆转铁蛋白摄取铁。
J Clin Invest. 1978 Nov;62(5):944-51. doi: 10.1172/JCI109223.
6
Preferential utilization in vitro of iron bound to diferric transferrin by rabbit reticulocytes.兔网织红细胞在体外对与双铁转铁蛋白结合的铁的优先利用。
Biochem J. 1977 Aug 15;166(2):175-9. doi: 10.1042/bj1660175.
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Studies on the forms of iron-transferrin released from rabbit reticulocytes.
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Iron-donating properties of transferrin.
Biochemistry. 1975 Jan 28;14(2):262-8. doi: 10.1021/bi00673a011.
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Evidence for the functional equivalence of the iron-binding sites of rat transferrin.大鼠转铁蛋白铁结合位点功能等效性的证据。
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Iron uptake from sialo transferrins by rat reticulocytes.大鼠网织红细胞从唾液酸转铁蛋白摄取铁。
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本文引用的文献

1
The determination of enzyme inhibitor constants.酶抑制剂常数的测定
Biochem J. 1953 Aug;55(1):170-1. doi: 10.1042/bj0550170.
2
The behavior of transferrin iron in the rat.转铁蛋白铁在大鼠体内的行为
Blood. 1981 Feb;57(2):218-28.
3
No functional difference of the two iron-binding sites of human transferrin in vitro.人转铁蛋白两个铁结合位点在体外无功能差异。
Clin Sci (Lond). 1981 Feb;60(2):185-90. doi: 10.1042/cs0600185.
4
Uptake and release of iron from human transferrin.铁从人转铁蛋白中的摄取与释放
Proc Natl Acad Sci U S A. 1981 Apr;78(4):2572-6. doi: 10.1073/pnas.78.4.2572.
5
Transferrin receptors and iron uptake during erythroid cell development.红系细胞发育过程中的转铁蛋白受体与铁摄取
Biochim Biophys Acta. 1982 May 7;687(2):204-10. doi: 10.1016/0005-2736(82)90547-8.
6
Interaction of human diferric transferrin with reticulocytes.人脱铁转铁蛋白与网织红细胞的相互作用。
Proc Natl Acad Sci U S A. 1981 Jan;78(1):621-5. doi: 10.1073/pnas.78.1.621.
7
An improved method for the simultaneous determination of iron-55 and iron-59 in blood by liquid scintillation counting.一种通过液体闪烁计数同时测定血液中55铁和59铁的改进方法。
Int J Appl Radiat Isot. 1966 Jul;17(7):391-7. doi: 10.1016/0020-708x(66)90065-2.
8
The effect of metal attachment to human apotransferrin on its binding to reticulocytes.
Biochim Biophys Acta. 1969 Nov 11;194(1):25-33. doi: 10.1016/0005-2795(69)90175-5.
9
An evaluation of adsorption methods for measurement of plasma iron-binding capacity.用于测量血浆铁结合能力的吸附方法评估。
J Lab Clin Med. 1970 Sep;76(3):497-506.
10
Iron-donating properties of transferrin.
Biochemistry. 1975 Jan 28;14(2):262-8. doi: 10.1021/bi00673a011.

脱铁转铁蛋白在将铁传递给网织红细胞方面的竞争优势。

Competitive advantage of diferric transferrin in delivering iron to reticulocytes.

作者信息

Huebers H A, Csiba E, Huebers E, Finch C A

出版信息

Proc Natl Acad Sci U S A. 1983 Jan;80(1):300-4. doi: 10.1073/pnas.80.1.300.

DOI:10.1073/pnas.80.1.300
PMID:6572005
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC393361/
Abstract

Radioiron- and radioiodine-labeled forms of human diferric and monoferric transferrin and apotransferrin, isolated by preparative isoelectric focusing, were used to define transferrin-iron uptake by human reticulocytes. In mixtures of human diferric and monoferric transferrin, the diferric molecule had a constant 7-fold advantage in delivering iron to reticulocytes, as compared with the 2-fold advantage when single solutions of mono- and diferric transferrins were compared. This was shown to be due to competitive interaction in iron delivery, probably at a common membrane-receptor binding site for transferrin. Apotransferrin did not interfere with the iron-donating process and its limited cellular uptake was inhibited in noncompetitive fashion by diferric transferrin.

摘要

通过制备性等电聚焦分离得到的人双铁和单铁转铁蛋白及脱铁转铁蛋白的放射性铁和放射性碘标记形式,被用于确定人网织红细胞对转铁蛋白-铁的摄取。在人双铁和单铁转铁蛋白的混合物中,与分别比较单铁和双铁转铁蛋白单一溶液时2倍的优势相比,双铁分子在将铁递送至网织红细胞方面具有恒定的7倍优势。这表明这是由于铁递送过程中的竞争性相互作用,可能是在转铁蛋白共同的膜受体结合位点。脱铁转铁蛋白不干扰铁的捐赠过程,其有限的细胞摄取受到双铁转铁蛋白非竞争性方式的抑制。