Nucleation of glucose isomerase protein crystals in a nonclassical disguise The role of crystalline precursors
Protein crystallization is an astounding feat of nature. Even though proteins are large, anisotropic molecules with complex, heterogeneous surfaces, they can spontaneously group into two-and three-dimensional arrays with high precision. And yet, the biggest hurdle in this assembly process, the forma...
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Published in | Proceedings of the National Academy of Sciences - PNAS Vol. 119; no. 7; pp. 1 - 6 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
United States
National Academy of Sciences
15.02.2022
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Subjects | |
Online Access | Get full text |
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Summary: | Protein crystallization is an astounding feat of nature. Even though proteins are large, anisotropic molecules with complex, heterogeneous surfaces, they can spontaneously group into two-and three-dimensional arrays with high precision. And yet, the biggest hurdle in this assembly process, the formation of a nucleus, is still poorly understood. In recent years, the two-step nucleation model has emerged as the consensus on the subject, but it still awaits extensive experimental verification. Here, we set out to reconstruct the nucleation pathway of the candidate protein glucose isomerase (GI), for which there have been indications that it may follow a two-step nucleation pathway under certain conditions. We find that the precursor phase present during the early stages of the reaction process is nanoscopic crystallites that have lattice symmetry equivalent to the mature crystals found at the end of a crystallization experiment. Our observations underscore the need for experimental data at a lattice-resolving resolution on other proteins so that a general picture of protein crystal nucleation can be formed. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 PMCID: PMC8851477 Edited by David Weitz, Department of Physics Division of Engineering and Applied Science, Harvard University, Cambridge, MA; received May 27, 2021; accepted December 20, 2021 Author contributions: A.E.S.V.D. and M.S. designed research; A.E.S.V.D., W.L.L., G.S., and M.S. performed research; A.E.S.V.D., W.L.L., G.S., and M.S. analyzed data; and A.E.S.V.D. and M.S. wrote the paper. |
ISSN: | 0027-8424 1091-6490 1091-6490 |
DOI: | 10.1073/pnas.2108674119 |