1y2m
From Proteopedia
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Crystal structure of phenylalanine ammonia-lyase from yeast Rhododporidium toruloides
Overview
Structure-based protein engineering coupled with chemical modifications, (e.g., pegylation) is a powerful combination to significantly improve the, development of proteins as therapeutic agents. As a test case, phenylalanine ammonia-lyase (PAL, EC 4.3.1.5) was selected for enzyme, replacement therapy in phenylketonuria [C.R. Scriver, S. Kaufman, Hyperphenylalaninemia:phenylalanine Hydroxylase Deficiency. The Metabolic, and Molecular Bases of Inherited Disease, McGraw-Hill, New York, 2001, Chapter 77], an inherited metabolic disorder (OMIM 261600) causing mental, retardation due to deficiency of the enzyme l-phenylalanine hydroxylase, (EC 1.14.16.1). Previous in vivo studies of recombinant PAL demonstrated a, lowering of blood l-phenylalanine levels; yet, the metabolic effect was, not sustained due to protein degradation and immunogenicity [C.N., Sarkissian, Z. Shao, F. Blain, R. Peevers, H. Su, R. Heft, T.M. Chang, C.R. Scriver, A different approach to treatment of, phenylketonuria:phenylalanine degradation with recombinant phenylalanine, ammonia lyase, Proc. Natl. Acad. Sci. USA 96 (1999) 2339; J.A. Hoskins, G., Jack, H.E. Wade, R.J. Peiris, E.C. Wright, D.J. Starr, J. Stern, Enzymatic, control of phenylalanine intake in phenylketonuria, Lancet 1 (1980) 392;, C.M. Ambrus, S. Anthone, C. Horvath, K. Kalghatgi, A.S. Lele, G. Eapen, J.L. Ambrus, A.J. Ryan, P. Li, Extracorporeal enzyme reactors for, depletion of phenylalanine in phenylketonuria, Ann. Intern. Med. 106, (1987) 531]. Here, we report the 1.6A three-dimensional structure of, Rhodosporidium toruloides PAL, structure-based molecular engineering, pegylation of PAL, as well as in vitro and in vivo PKU mouse model studies, on pegylated PAL formulations. Our results show that pegylation of R., toruloides PAL leads to promising therapeutic efficacy after subcutaneous, injection by enhancing the in vivo activity, lowering plasma, phenylalanine, and leading to reduced immunogenicity. The, three-dimensional structure of PAL provides a basis for understanding the, properties of pegylated forms of PAL and strategies for structure-based, re-engineering of PAL for PKU treatment.
About this Structure
1Y2M is a Single protein structure of sequence from Rhodosporidium toruloides. Active as Phenylalanine ammonia-lyase, with EC number 4.3.1.5 Full crystallographic information is available from OCA.
Reference
Structure-based chemical modification strategy for enzyme replacement treatment of phenylketonuria., Wang L, Gamez A, Sarkissian CN, Straub M, Patch MG, Han GW, Striepeke S, Fitzpatrick P, Scriver CR, Stevens RC, Mol Genet Metab. 2005 Sep-Oct;86(1-2):134-40. Epub 2005 Jul 11. PMID:16006165
Page seeded by OCA on Wed Nov 21 06:31:13 2007