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6Z60

The RSL - sulfonato-calix[8]arene complex, P213 form, CAPS pH 9.5

Summary for 6Z60
Entry DOI10.2210/pdb6z60/pdb
Related6STH 6Z5G 6Z5M 6Z5P 6Z5Q 6Z5W 6Z5X
DescriptorFucose-binding lectin protein, sulfonato-calix[8]arene, SULFATE ION, ... (5 entities in total)
Functional Keywordscalixarene, protein framework, cage, crystal engineering, molecular glue, synthetic receptor, macrocycle, biomaterial, sugar binding protein
Biological sourceRalstonia solanacearum
Total number of polymer chains1
Total formula weight11679.42
Authors
Ramberg, K.,Engilberge, S.,Crowley, P.B. (deposition date: 2020-05-27, release date: 2021-04-14, Last modification date: 2024-01-24)
Primary citationRamberg, K.O.,Engilberge, S.,Skorek, T.,Crowley, P.B.
Facile Fabrication of Protein-Macrocycle Frameworks.
J.Am.Chem.Soc., 143:1896-1907, 2021
Cited by
PubMed Abstract: Precisely defined protein aggregates, as exemplified by crystals, have applications in functional materials. Consequently, engineered protein assembly is a rapidly growing field. Anionic calix[n]arenes are useful scaffolds that can mold to cationic proteins and induce oligomerization and assembly. Here, we describe protein-calixarene composites obtained via cocrystallization of commercially available sulfonato-calix[8]arene () with the symmetric and "neutral" protein RSL. Cocrystallization occurred across a wide range of conditions and protein charge states, from pH 2.2-9.5, resulting in three crystal forms. Cationization of the protein surface at pH ∼ 4 drives calixarene complexation and yielded two types of porous frameworks with pore diameters >3 nm. Both types of framework provide evidence of protein encapsulation by the calixarene. Calixarene-masked proteins act as nodes within the frameworks, displaying octahedral-type coordination in one case. The other framework formed millimeter-scale crystals within hours, without the need for precipitants or specialized equipment. NMR experiments revealed macrocyclemodulated side chain p values and suggested a mechanism for pH-triggered assembly. The same low pH framework was generated at high pH with a permanently cationic arginine-enriched RSL variant. Finally, in addition to protein framework fabrication, enables structure determination.
PubMed: 33470808
DOI: 10.1021/jacs.0c10697
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.166 Å)
Structure validation

226707

数据于2024-10-30公开中

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