共 28 条
Identification of a cofilin-like actin-binding site on translationally controlled tumor protein (TCTP)
被引:41
作者:

Tsarova, Katsiaryna
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h-index: 0
机构: Univ Florida, Dept Med, Div Rheumatol & Clin Immunol, Gainesville, FL 32610 USA

Yarmola, Elena G.
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h-index: 0
机构: Univ Florida, Dept Med, Div Rheumatol & Clin Immunol, Gainesville, FL 32610 USA

Bubb, Michael R.
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h-index: 0
机构:
Univ Florida, Dept Med, Div Rheumatol & Clin Immunol, Gainesville, FL 32610 USA Univ Florida, Dept Med, Div Rheumatol & Clin Immunol, Gainesville, FL 32610 USA
机构:
[1] Univ Florida, Dept Med, Div Rheumatol & Clin Immunol, Gainesville, FL 32610 USA
关键词:
Cofilin;
Translationally controlled tumor protein;
Actin;
DEPOLYMERIZING FACTOR;
FILAMENT TURNOVER;
CANCER-CELLS;
IN-VITRO;
ADF/COFILIN;
MIGRATION;
REVERSION;
PROFILIN;
MOTILITY;
D O I:
10.1016/j.febslet.2010.10.054
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
070307 [化学生物学];
071010 [生物化学与分子生物学];
摘要:
Translationally controlled tumor protein (TCTP) expression is suppressed during cancer cell reversion to a non-malignant phenotype. We identified a primary sequence of TCTP with homology to ADF/cofilin. We confirm that a synthetic peptide corresponding to this sequence binds specifically to actin and is displaced from actin by cofilin. TCTP peptide has higher affinity for G-actin than F-actin and does not block actin-filament depolymerization by cofilin. These results suggest that TCTP may channel active cofilin to F-actin, enhancing the cofilin-activity cycle in invasive tumor cells. Loss of TCTP may result in sequestration of active cofilin by a monomeric pool of actin. Published by Elsevier B.V. on behalf of the Federation of European Biochemical Societies.
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页码:4756 / 4760
页数:5
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