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| ==Synthetic nanobody in complex with MBP== | | ==Synthetic nanobody in complex with MBP== |
- | <StructureSection load='5m13' size='340' side='right' caption='[[5m13]], [[Resolution|resolution]] 1.37Å' scene=''> | + | <StructureSection load='5m13' size='340' side='right'caption='[[5m13]], [[Resolution|resolution]] 1.37Å' scene=''> |
| == Structural highlights == | | == Structural highlights == |
- | <table><tr><td colspan='2'>[[5m13]] is a 2 chain structure with sequence from [http://en.wikipedia.org/wiki/Ecoli Ecoli] and [http://en.wikipedia.org/wiki/Synthetic_construct_sequences Synthetic construct sequences]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5M13 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5M13 FirstGlance]. <br> | + | <table><tr><td colspan='2'>[[5m13]] is a 2 chain structure with sequence from [https://en.wikipedia.org/wiki/Escherichia_coli_K-12 Escherichia coli K-12] and [https://en.wikipedia.org/wiki/Synthetic_construct Synthetic construct]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5M13 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=5M13 FirstGlance]. <br> |
- | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=EDO:1,2-ETHANEDIOL'>EDO</scene></td></tr> | + | </td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 1.372Å</td></tr> |
- | <tr id='gene'><td class="sblockLbl"><b>[[Gene|Gene:]]</b></td><td class="sblockDat">malE, b4034, JW3994 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=83333 ECOLI])</td></tr> | + | <tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=EDO:1,2-ETHANEDIOL'>EDO</scene></td></tr> |
- | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5m13 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5m13 OCA], [http://pdbe.org/5m13 PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=5m13 RCSB], [http://www.ebi.ac.uk/pdbsum/5m13 PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=5m13 ProSAT]</span></td></tr> | + | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=5m13 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5m13 OCA], [https://pdbe.org/5m13 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=5m13 RCSB], [https://www.ebi.ac.uk/pdbsum/5m13 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=5m13 ProSAT]</span></td></tr> |
| </table> | | </table> |
| == Function == | | == Function == |
- | [[http://www.uniprot.org/uniprot/MALE_ECOLI MALE_ECOLI]] Involved in the high-affinity maltose membrane transport system MalEFGK. Initial receptor for the active transport of and chemotaxis toward maltooligosaccharides. | + | [https://www.uniprot.org/uniprot/MALE_ECOLI MALE_ECOLI] Involved in the high-affinity maltose membrane transport system MalEFGK. Initial receptor for the active transport of and chemotaxis toward maltooligosaccharides. |
| <div style="background-color:#fffaf0;"> | | <div style="background-color:#fffaf0;"> |
| == Publication Abstract from PubMed == | | == Publication Abstract from PubMed == |
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| ==See Also== | | ==See Also== |
- | *[[Maltose-binding protein|Maltose-binding protein]] | + | *[[Maltose-binding protein 3D structures|Maltose-binding protein 3D structures]] |
| == References == | | == References == |
| <references/> | | <references/> |
| __TOC__ | | __TOC__ |
| </StructureSection> | | </StructureSection> |
- | [[Category: Ecoli]] | + | [[Category: Escherichia coli K-12]] |
- | [[Category: Synthetic construct sequences]] | + | [[Category: Large Structures]] |
- | [[Category: Egloff, P]] | + | [[Category: Synthetic construct]] |
- | [[Category: Seeger, M A]] | + | [[Category: Egloff P]] |
- | [[Category: Zimmermann, I]] | + | [[Category: Seeger MA]] |
- | [[Category: Immune system]]
| + | [[Category: Zimmermann I]] |
- | [[Category: Maltose binding protein]]
| + | |
- | [[Category: Nanobody]]
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- | [[Category: Synthetic library]]
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| Structural highlights
Function
MALE_ECOLI Involved in the high-affinity maltose membrane transport system MalEFGK. Initial receptor for the active transport of and chemotaxis toward maltooligosaccharides.
Publication Abstract from PubMed
Mechanistic and structural studies of membrane proteins require their stabilization in specific conformations. Single domain antibodies are potent reagents for this purpose, but their generation relies on immunizations, which impedes selections in the presence of ligands typically needed to populate defined conformational states. To overcome this key limitation, we developed an in vitro selection platform based on synthetic single domain antibodies named sybodies. To target the limited hydrophilic surfaces of membrane proteins, we designed three sybody libraries that exhibit different shapes and moderate hydrophobicity of the randomized surface. A robust binder selection cascade combining ribosome and phage display enabled the generation of conformation-selective, high affinity sybodies against an ABC transporter and two previously intractable human SLC transporters, GlyT1 and ENT1. The platform does not require access to animal facilities and builds exclusively on commercially available reagents, thus enabling every lab to rapidly generate binders against challenging membrane proteins.
Synthetic single domain antibodies for the conformational trapping of membrane proteins.,Zimmermann I, Egloff P, Hutter CA, Arnold FM, Stohler P, Bocquet N, Hug MN, Huber S, Siegrist M, Hetemann L, Gera J, Gmur S, Spies P, Gygax D, Geertsma ER, Dawson RJ, Seeger MA Elife. 2018 May 24;7. pii: 34317. doi: 10.7554/eLife.34317. PMID:29792401[1]
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.
See Also
References
- ↑ Zimmermann I, Egloff P, Hutter CA, Arnold FM, Stohler P, Bocquet N, Hug MN, Huber S, Siegrist M, Hetemann L, Gera J, Gmur S, Spies P, Gygax D, Geertsma ER, Dawson RJ, Seeger MA. Synthetic single domain antibodies for the conformational trapping of membrane proteins. Elife. 2018 May 24;7. pii: 34317. doi: 10.7554/eLife.34317. PMID:29792401 doi:http://dx.doi.org/10.7554/eLife.34317
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