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Carla P. Guimaraes

Researcher at Massachusetts Institute of Technology

Publications -  27
Citations -  5838

Carla P. Guimaraes is an academic researcher from Massachusetts Institute of Technology. The author has contributed to research in topics: Sortase & Sortase A. The author has an hindex of 21, co-authored 27 publications receiving 5168 citations.

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M13 bacteriophage display framework that allows sortase-mediated modification of surface-accessible phage proteins.

TL;DR: In this article, the authors exploit bacterial sortases to attach a variety of moieties to the capsid proteins of M13 bacteriophage, which can be functionalized with entities ranging from small molecules (e.g., fluorophores, biotin) to correctly folded proteins (e., GFP, antibodies, streptavidin) in site-specific manner, and with yields that surpass those of any reported using phage display technology.
Journal ArticleDOI

Identification of host cell factors required for intoxication through use of modified cholera toxin

TL;DR: A novel labeling strategy is applied to cholera toxin subunit A1 in the context of a pre-assembled holotoxin allowing tracking of its intracellular trafficking pathway and identification of host proteins involved in cell intoxication.
Patent

Methods for ligation and uses thereof

TL;DR: In this paper, a transamidase recognition sequence that allows ligating an acyl donor compound with a nucleophilic acyl acceptor in the presence of transamic acid was presented.
Journal ArticleDOI

Production of unnaturally linked chimeric proteins using a combination of sortase-catalyzed transpeptidation and click chemistry

TL;DR: By equipping the N terminus or C terminus of the proteins of interest with a set of click handles using sortase A, followed by a strain-promoted click reaction, unnatural N- to-N and C-to-C linked (hetero) fusion proteins are established.
Journal ArticleDOI

GPR107, a G-protein-coupled Receptor Essential for Intoxication by Pseudomonas aeruginosa Exotoxin A, Localizes to the Golgi and Is Cleaved by Furin

TL;DR: A genome-wide genetic screen in human KBM7 cells was performed to uncover host factors used by PE, several of which were confirmed by CRISPR/Cas9-gene editing in a different cell type, including GPR107, an orphan G-protein-coupled receptor.