University home >
Biochemistry > People > Dr Andrea Brancaccio
Browse/search for people
Dr Andrea Brancaccio
Selected publications
- Dempsey, C, Bigotti, MG, Adams, J & Brancaccio, A, 2019, ‘Analysis of α-dystroglycan/LG domain binding modes: investigating protein motifs that regulate the affinity of isolated LG domains’. Frontiers in Molecular Biosciences, vol 6.
- Brancaccio, A, 2019, ‘A molecular overview of the primary dystroglycanopathies’. Journal of Cellular and Molecular Medicine, vol 23., pp. 3058-3062
- Shoemark, D, Sessions, R, Brancaccio, A & Bigotti, MG, 2018, ‘Intraring allostery controls the function and assembly of a hetero-oligomeric class II chaperonin’. FASEB Journal, vol 32., pp. 2223-2234
- Paul, DM, Beuron, F, Sessions, RB, Brancaccio, A & Bigotti, G, 2016, ‘Internal (His)6-tagging delivers a fully functional hetero-oligomeric class II chaperonin in high yield’. Scientific Reports, vol 6.
- Adams, J & Brancaccio, A, 2015, ‘The evolution of the dystroglycan complex, a major mediator of muscle integrity’. Biology Open, vol 4., pp. 1163-1179
Latest publications
- Signorino, G, Covaceuszach, S, Bozzi, M, Hubner, W, Mönkemöller, V, Konarev, PV, Cassetta, A, Brancaccio, A & Sciandra, F, 2018, ‘A dystroglycan mutation (p.Cys667Phe) associated to muscle-eye-brain disease with multicystic leucodystrophy results in ER-retention of the mutant protein’. Human Mutation, vol 39., pp. 266-280
- Gioia, M, Fasciglione, GF, Sbardella, D, Sciandra, F, Casella, M, Camerini, S, Crescenzi, M, Gori, A, Tarantino, U, Cozza, P, Brancaccio, A, Coletta, M & Bozzi, M, 2018, ‘The enzymatic processing of α-dystroglycan by MMP-2 is controlled by two anchoring sites distinct from the active site’. PLoS ONE, vol 13., pp. e0192651
- Covaceuszach, S, Bozzi, M, Bigotti, MG, Sciandra, F, Konarev, PV, Brancaccio, A & Cassetta, A, 2017, ‘Structural flexibility of human α-dystroglycan’. FEBS Open Bio, vol 7., pp. 1064-1077
- Covaceuszach, S, Bozzi, M, Bigotti, MG, Sciandra, F, Konarev, PV, Brancaccio, A & Cassetta, A, 2017, ‘The effect of the pathological V72I, D109N and T190M missense mutations on the molecular structure of α-dystroglycan’. PLoS ONE, vol 12.
- Brancaccio, A & Adams, JC, 2017, ‘An evaluation of the evolution of the gene structure of dystroglycan’. BMC Research Notes, vol 10.
View complete publications list in the University of Bristol publications system
