A study of intrinsic disorder and its role in functional proteomics

The last decade has witnessed the emergence of an alternate view on how protein function arises. This view attributes the functionality of many proteins to the presence of an ensemble of flexible regions popularly as `intrinsically disordered' or `unstructured'. Several proteomic studies have corroborated the existence of either wholly disordered proteins or proteins that contain regions of disorder in them. The purpose of this dissertation was to investigate the consistency of such regions across experiments, their mechanism of facilitating function via disorder-to-order transitions, their presence and significance in pathogenic versus non-pathogenic organisms and their promise of applicability towards the computational prediction of peptides involved in the most common class of post-translational modifications, phosphorylation. Besides these, a new algorithm exploiting the strong correlation between phosphorylation and intrinsic disorder has also been proposed to improve the detection of phosphorylated peptides via high-throughput methods such as tandem mass-spectrometry (LC-MS/MS). Results presented in this study, guide us in understanding the robustness of unstructured regions in proteins to sequence changes and environment, their role in facilitating molecular recognition as well as improving currently available methods for identification of post-translationally modified peptides. The findings and conclusions of this dissertation have the potential to impact ongoing structural genomics initiatives by suggesting alternative methods for determining structure for targets containing regions of disorder. Additional ramifications of results from this work include directing attention towards the possible use of regions of intrinsic disorder by pathogenic organisms for host cell invasion. We believe that unlike the traditional reductionist approach in a scientific method, this study gathers strength and utility by investigating the role of intrinsic disorder on more than one front in order to provide a novel perspective to the understanding of complex interactions within biological systems. Concluding arguments presented in this study pique one's curiosity regarding the evolution of disordered regions and proteins in general. On a technological side, the findings from this study unequivocally support the viable use of informatics methods in gaining new insights about a relatively young class of proteins known as intrinsically disordered proteins and its applicability to improve our present knowledge of cellular physiology.

Grantor dc:publisher

[Bloomington, Ind.] : Indiana University

Year dc:date.issued

2009

Author dc:creator

• Mohan, Amrita

Advisor dc:contributor.advisor

• Radivojac, Predrag

• functional proteomics
• intrinsic disorder
• mass-spectrometry
• molecular recognition
• pathogens
• reproducibility

Statement dc:rights

• Attribution Non-commercial Share Alike (by-nc-sa)

Licence dc:rights.uri

• http://creativecommons.org/licenses/by-nc-sa/4.0/

Language dc:language.iso

EN

Handle dc:identifier.uri

https://hdl.handle.net/2022/8917

OAI identifier oai:identifier

oai:scholarworks.iu.edu:2022/8917