纯度 | >90%SDS-PAGE. |
种属 | E.coli |
靶点 | mutL |
Uniprot No | P23367 |
内毒素 | < 0.01EU/μg |
表达宿主 | E.coli |
表达区间 | 1-615aa |
氨基酸序列 | MPIQVLPPQLANQIAAGEVVERPASVVKELVENSLDAGATRIDIDIERGGAKLIRIRDNGCGIKKDELALALARHATSKIASLDDLEAIISLGFRGEALASISSVSRLTLTSRTAEQQEAWQAYAEGRDMNVTVKPAAHPVGTTLEVLDLFYNTPARRKFLRTEKTEFNHIDEIIRRIALARFDVTINLSHNGKIVRQYRAVPEGGQKERRLGAICGTAFLEQALAIEWQHGDLTLRGWVADPNHTTPALAEIQYCYVNGRMMRDRLINHAIRQACEDKLGADQQPAFVLYLEIDPHQVDVNVHPAKHEVRFHQSRLVHDFIYQGVLSVLQQQLETPLPLDDEPQPAPRSIPENRVAAGRNHFAEPAAREPVAPRYTPAPASGSRPAAPWPNAQPGYQKQQGEVYRQLLQTPAPMQKLKAPEPQEPALAANSQSFGRVLTIVHSDCALLERDGNISLLSLPVAERWLRQAQLTPGEAPVCAQPLLIPLRLKVSAEEKSALEKAQSALAELGIDFQSDAQHVTIRAVPLPLRQQNLQILIPELIGYLAKQSVFEPGNIAQWIARNLMSEHAQWSMAQAITLLADVERLCPQLVKTPPGGLLQSVDLHPAIKALKDE |
预测分子量 | 71.9kDa |
蛋白标签 | His tag N-Terminus |
缓冲液 | PBS, pH7.4, containing 0.01% SKL, 1mM DTT, 5% Trehalose and Proclin300. |
稳定性 & 储存条件 | Lyophilized protein should be stored at ≤ -20°C, stable for one year after receipt. Reconstituted protein solution can be stored at 2-8°C for 2-7 days. Aliquots of reconstituted samples are stable at ≤ -20°C for 3 months. |
复溶 | Always centrifuge tubes before opening.Do not mix by vortex or pipetting. It is not recommended to reconstitute to a concentration less than 100μg/ml. Dissolve the lyophilized protein in distilled water. Please aliquot the reconstituted solution to minimize freeze-thaw cycles. |
以下是关于mutL重组蛋白的3篇代表性文献摘要:
1. **"Structure of the MutL C-terminal domain: A model of intact MutL ATPase"**
*Guarné, A., et al. (2000). Journal of Molecular Biology*
该研究解析了大肠杆菌MutL蛋白C端结构域的三维结构,揭示了其ATP酶活性机制,并提出了MutL通过ATP依赖的构象变化调控DNA错配修复的模型。
2. **"Functional analysis of the MutL protein from Thermus thermophilus in mismatch repair"**
*Fukui, K., et al. (2008). Nucleic Acids Research*
作者纯化了嗜热菌来源的重组MutL蛋白,发现其具有ATP水解活性,并在体外实验中证明MutL通过结合MutS-错配DNA复合物激活下游修复核酸内切酶活性。
3. **"MutL traps MutS at a DNA mismatch"**
*Hargreaves, V.V., et al. (2010). Nature Structural & Molecular Biology*
研究利用重组MutL和MutS蛋白的体外实验,证明MutL通过稳定MutS与DNA错配位点的结合,增强修复复合物的组装效率,并协调修复信号传递。
4. **"Dissection of the ATPase activity of E. coli MutL and its role in mismatch repair"**
*Ban, C., & Yang, W. (1998). EMBO Journal*
通过构建大肠杆菌重组MutL突变体,发现其ATP酶活性对修复功能至关重要,并揭示ATP结合/水解循环驱动MutL二聚化及与MutH核酸内切酶的相互作用。
**Background of MutL Recombinant Protein**
MutL is a conserved DNA repair protein central to the mismatch repair (MMR) system, a critical pathway for maintaining genomic stability by correcting replication errors and preventing mutagenesis. In *E. coli*, MutL functions as a homodimer, partnering with MutS and MutH to recognize and repair mismatches or small insertion/deletion loops during DNA replication. MutS first detects mismatches, triggering MutL’s ATPase activity to coordinate downstream repair steps. MutL acts as a molecular scaffold, recruiting endonucleases like MutH to nick the daughter strand, enabling excision and resynthesis of the error-containing DNA segment.
In eukaryotes, MutL homologs (e.g., MLH1. PMS2. MLH3) form heterodimers (e.g., MLH1-PMS2) that are essential for MMR. These proteins also interact with replication machinery and participate in meiotic recombination. Defects in human MutL homologs are linked to hereditary cancers, notably Lynch syndrome, characterized by microsatellite instability due to impaired MMR.
Recombinant MutL proteins are engineered for *in vitro* studies to dissect MMR mechanisms, screen for mutations in cancer diagnostics, or evaluate chemotherapeutic responses. Produced via bacterial or eukaryotic expression systems, recombinant MutL retains functional domains for protein-DNA/protein interactions and ATP hydrolysis. Its applications extend to synthetic biology, where MutL variants are explored to enhance gene-editing tools like CRISPR by improving precision. Research on MutL continues to advance understanding of DNA repair, cancer biology, and antimicrobial strategies targeting bacterial MMR pathways.
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