首页> 外文期刊>The biochemical journal >Relaxin-like factor (RLF)/insulin-like peptide 3 (INSL3) is secreted from testicular Leydig cells as a monomeric protein comprising three domains B–C–A with full biological activity in boars
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Relaxin-like factor (RLF)/insulin-like peptide 3 (INSL3) is secreted from testicular Leydig cells as a monomeric protein comprising three domains B–C–A with full biological activity in boars

机译:松弛素样因子(RLF)/胰岛素样肽3(INSL3)作为一种单体蛋白从睾丸Leydig细胞分泌,该蛋白包含三个结构域B–C–A,在公猪中具有完全的生物学活性

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摘要

RLF (relaxin-like factor), also known as INSL3 (insulin-like peptide 3), is a novel member of the relaxin/insulin gene family that is expressed in testicular Leydig cells. Despite the implicated role of RLF/INSL3 in testis development, its native conformation remains unknown. In the present paper we demonstrate for the first time that boar testicular RLF/INSL3 is isolated as a monomeric structure with full biological activity. Using a series of chromatography steps, the native RLF/INSL3 was highly purified as a single peak in reverse-phase HPLC. MS/MS (tandem MS) analysis of the trypsinized sample provided 66% sequence coverage and revealed a distinct monomeric structure consisting of the B-, C- and A-domains deduced previously from the RLF/INSL3 cDNA. Moreover, the N-terminal peptide was four amino acid residues longer than predicted previously. MS analysis of the intact molecule and PMF (peptide mass fingerprinting) analysis at 100% sequence coverage confirmed this structure and indicated the existence of three site-specific disulfide bonds. RLF/INSL3 retained full bioactivity in HEK (human embryonic kidney)-293 cells expressing RXFP2 (relaxin/insulin-like family peptide receptor 2), the receptor for RLF/INSL3. Furthermore, RLF/INSL3 was found to be secreted from Leydig cells into testicular venous blood. Collectively, these results indicate that boar RLF/INSL3 is secreted from testicular Leydig cells as a B–C–A monomeric structure with full biological activity.Abbreviations: ACN, acetonitrile; DIG, digoxigenin; ECL, enhanced chemiluminescence; HEK, human embryonic kidney; INSL3, insulin-like peptide 3; MALDI, matrix-assisted laser desorption ionization; MS/MS, tandem MS; PC1/3, prohormone convertase 1/3; PMF, peptide mass fingerprinting; RLF, relaxin-like factor; RXFP2, relaxin/insulin-like family peptide receptor 2; TBST-milk, Tris-buffered saline containing Tween 20 with 2% skimmed milk; TF, transferrin; TFA, trifluoroacetic acid; TR-FIA, time-resolved fluoroimmunoassay
机译:RLF(松弛素样因子),也称为INSL3(胰岛素样肽3),是在睾丸Leydig细胞中表达的松弛素/胰岛素基因家族的新成员。尽管RLF / INSL3在睾丸发育中有牵连的作用,其天然构象仍然未知。在本文中,我们首次证明公猪睾丸RLF / INSL3是具有完整生物活性的单体结构。使用一系列色谱步骤,天然RLF / INSL3在反相HPLC中作为单个峰被高度纯化。胰蛋白酶消化样品的MS / MS(串联MS)分析提供了66%的序列覆盖率,并揭示了由先前从RLF / INSL3 cDNA推导的B,C和A结构域组成的独特单体结构。而且,N端肽比以前预测的长四个氨基酸残基。完整分子的MS分析和100%序列覆盖率的PMF(肽质量指纹分析)分析证实了这种结构,并表明存在三个位点特异性二硫键。 RLF / INSL3在表达RXFP2(松弛素/胰岛素样家族肽受体2)(RLF / INSL3的受体)的HEK(人胚肾)-293细胞中保留了全部生物活性。此外,发现RLF / INSL3从Leydig细胞分泌到睾丸静脉血中。总体而言,这些结果表明,公猪RLF / INSL3以具有完全生物学活性的B–C–A单体结构形式从睾丸Leydig细胞分泌。地高辛,地高辛ECL,增强化学发光; HEK,人类胚胎肾脏; INSL3,胰岛素样肽3; MALDI,基质辅助激光解吸电离; MS / MS,串联MS; PC1 / 3,激素原转化酶1/3; PMF,肽质量指纹图谱; RLF,松弛素样因子; RXFP2,松弛素/胰岛素样家族肽受体2; TBST牛奶,Tris缓冲盐水,含Tween 20和2%脱脂牛奶; TF,转铁蛋白; TFA,三氟乙酸; TR-FIA,时间分辨荧光免疫分析

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