Antonio C. B. Burtoloso

Prof. Dr. Antonio C. B. Burtoloso

orcid

Research Focus & Metrics

Academic Career Length

23Years (2004-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

View All Publications
1 July 2013 in European Journal of Organic Chemistry
Verified
Journal Article
Closed access
PDF file
ABAntonio C. B. Burtoloso
Antonio C. B. Burtoloso
RDRafael M. P. Dias
Rafael M. P. Dias
ILIves A. Leonarczyk
Ives A. Leonarczyk

26 October 2016 in Nature Communications
Verified
Journal Article
Open access
BBBarbara Bernardim
Barbara Bernardim
PCPedro M.S.D. Cal
Pedro M.S.D. Cal
MMMaria Matos
Maria Matos
BOBruno Oliveira
Bruno Oliveira
NMNuria Martínez-Sáez
Nuria Martínez-Sáez
GBGonçalo J. L. Bernardes
Gonçalo J. L. Bernardes
Maleimides remain the reagents of choice for the preparation of therapeutic and imaging protein conjugates despite the known instability of the resulting products that undergo thiol-exchange reactions in vivo. Here we present the rational design of carbonylacrylic reagents for chemoselective cysteine bioconjugation. These reagents undergo rapid thiol Michael-addition under biocompatible conditions in stoichiometric amounts. When using carbonylacrylic reagents equipped with PEG or fluorophore moieties, this method enables access to protein and antibody conjugates precisely modified at pre-determined sites. Importantly, the conjugates formed are resistant to degradation in plasma and are biologically functional, as demonstrated by the selective imaging and detection of apoptotic and HER2+ cells, respectively. The straightforward preparation, stoichiometric use and exquisite cysteine selectivity of the carbonylacrylic reagents combined with the stability of the products and the availability of biologically relevant cysteine-tagged proteins make this method suitable for the routine preparation of chemically defined conjugates for in vivo applications.

1 July 2008 in Natural Product Reports
Verified
Journal Article
Closed access
PDF file
RBRoberto G. S. Berlinck
Roberto G. S. Berlinck
ABAntonio C. B. Burtoloso
Antonio C. B. Burtoloso
MKMiriam H. Kossuga
Miriam H. Kossuga
Covering: 2005 to 2007. Previous review: Nat. Prod. Rep., 2005, 22, 516. Organic guanidine compounds are reviewed, with emphasis on natural products isolation, identification, synthesis and biological activities. The literature survey includes purely synthetic guanidine derivatives, guanidine alkaloids and non-ribosomal peptides from bacteria and cyanobacteria, as well as related compounds isolated from marine and terrestrial invertebrates and higher plants.

8 December 2021 in Chemical Science
Verified
Journal Article
Open access
PDF file
CCClarice A. D. Caiuby
Clarice A. D. Caiuby
LFLucas G. Furniel
Lucas G. Furniel
ABAntonio C. B. Burtoloso
Antonio C. B. Burtoloso
Asymmetric transformations involving sulfoxonium ylides, culminating in catalytic enantioselective versions, are discussed in this perspective.


18 October 2010 in Natural Product Reports
Verified
Journal Article
Closed access
PDF file
RBRoberto G. S. Berlinck
Roberto G. S. Berlinck
ABAntonio C. B. Burtoloso
Antonio C. B. Burtoloso
ATAmaro E. Trindade-Silva
Amaro E. Trindade-Silva
SRStelamar Romminger
Stelamar Romminger
RMRaquel P. Morais
Raquel P. Morais
CMCarolina M. Mizuno
Carolina M. Mizuno
Covering: 2008 and 2009. Previous review: Nat. Prod. Rep., 2008, 25, 919 Organic guanidine compounds are reviewed, with emphasis on natural product isolation, identification, synthesis, biosynthesis and biological activities. The literature survey includes purely synthetic guanidine derivatives, guanidine alkaloids and non-ribosomal peptides from bacteria and cyanobacteria, as well as related compounds isolated from marine and terrestrial invertebrates and higher plants.